Glucan chain length domains

ABSTRACT

The invention relates to a method for changing the glucan chain lengths using fusion protein domains of various starch synthase enzymes in any starch or starch granule producing organism. The invention relates to identification of a GLucan ASSociation domain (herein after referred to as “GLASS” domain) of granule bound starch synthase (GBSS) used in combination with any other GLYcosyl TRransferase domain otherwise referred to as pfam00534-catalytic domain (herein after referred to as “GLYTR” domain) of one or more of any of the other starch synthase enzymes. The invention relates to identifying and using the new and surprising discovery that starch synthases are composed of at least two distinct functional domains herein after labeled as “GLASS” and “GLYTR”. More specifically, this invention relates to the genetic constructs that encode the fusions of the above domains and to the plants transformed with said constructs. The method of invention can thus be used in particular to provide a modified profile of starch granule associated starch synthase (SS) enzymes and by which modified glucan chain lengths of amylopectin and hence, modified starches and or complexes will be generated. This can be done in any organism and more particularly any plant that stores or synthesizes starch in any of its parts, such as potato, sweet potato, cassaya, pea, taro, banana, yam and cereal crops such as rice, maize, wheat, barley, oats, and sorghum.

[0001] This application claims priority to provisional patent application serial No. 60/279,720 filed Mar. 30, 2001, the entire contents of which is incorporated herein by reference.

[0002] The development of genetic engineering techniques has made it possible to transfer genes from various organisms and plants into other organisms or plants. Although starch has been altered by transformation and mutagenesis in the past, there is still a great need for further starch M modifications in order to meet the ever-increasing industrial need for variations of this natural polymer. Toward this end, there is a need to manipulate the chain lengths of glucan chains in amylopectin in order to provide novel starches with multitude of industrial uses. In order to achieve this goal the present invention is directed at introducing changes in the ratios, composition, and functionality of various enzymes in the starch synthesis pathway.

[0003] The present invention relates to novel plants expressing transgenic genes and having an altered ability to produce specialty starch traits with modified glucan chain lengths. Modification of starch biosynthesis pathways by changing the functionality of starch synthase enzymes has an enormous potential for production of new and improved starches. Maize starch is used to produce a wide range of food products (for human and animal consumption) and several industrial products. Several crop varieties are known which produce different types of starch. The type or quality of starch makes it suitable for certain purposes, including particular methods of processing or particular end-uses. For example, U.S. Pat. Nos. 4,789,557, 4,790,997, 4,774,328, 4,770,710, 4,798,735, 4,767,849, 4,801,470, 4,789,738, 4,792,458 and 5,009,911 describe naturally occurring maize mutants producing starches of differing fine structure suitable for use in various food products. Although known mutants produce altered starch, some of these lines are not suitable for crop breeding and/or for the farmers' purposes. By combining various mutants together, such as double, triple and quadruple mutants it is possible to create a variety of plant starches. One key element that is lacking in these starches is the ability to control glucan chain length in the amylopectin molecule. Moreover, such mutant plants often give relatively poor yields and also low gemination rates.

[0004] Glucan chain length and chain length distribution are the two key components that determine the functionality of any given starch. Glucan chain lengths can be modified by genetic manipulation of enzymes known to possess other favorable characteristics. For example, by manipulating the function and expression levels of one or more starch synthesizing enzyme genes in a plant, it is possible to significantly alter the type of starch produced. The present invention has led to a new undertstanding of how different starch synthase (SS) enzymes recognize and have specific catalytic capabilities to various lengths of glucan chains (See also, Commuri and Keeling, 2001, The Plant Journal, 25(5), 475-486; and Commuri et al., 2002, in review, The Plant Journal). Comparative analysis have recently been completed on the functionality and catalytic properties of various maize starch synthase enzymes, namely, SSI, SSIIa, SSIIb, granule bound starch synthase (GBSS), and Du1 (SSIII) using glucan substrates with varying average chain lengths (FIGS. 1, 2 &3). Each one of these enzymes possessed different glucan chain length specificities. In maize endosperm, not all the SS enzymes are expressed at the same levels nor localized uniformly in the amyloplast stroma, and/or starch granules. Thus, each form of SS enzyme must contribute in a unique and a specific way in setting the starch structure, and there exists an enormous potential to bring a modification to the structure of starch by alteration of their location of expression and manipulating the levels of activity of these enzymes in the endosperm. Of the five different SS enzymes known to date in maize, GBSS enzyme has the highest affinity to amylopectin followed by SSI (Table 1). It is because of this affinity for its glucan substrate that most of the protein entrapped in the starch granules is comprised of GBSS (˜60%) and SSI enzymes (FIG. 4). Enzymes like SSIIa or SSIIb are undetectable in the granule and are present in low amounts in the amyloplast stroma. The Du1 protein is barely detectable in the granules and is found in reasonable amounts in the amyloplast stroma. Different forms of starch synthases are broadly conserved in evolution and it is reasonable to propose that specific functions have been selected for each one of these isoforms (Myers et al., 2000). For example, in the dull1 (Wang et al., 1993) and sugary 2 (Takeda and Preiss, 1993) mutants that affect enzymes other than SSI (Gao et al., 1998, Harn et al., 1998), both mutations decrease the proportion of the intermediate and average length of long chains (B2 and B3) in the B amylopectin relative to the short (A and B1) chains. This suggests that the enzymes other than SSI are relatively less needed for synthesis of short chains, but are needed for the synthesis of intermediate and longer chains. Furthermore, dull 1 mutation in maize eliminates SS III and the amylopectin from this mutant endosperm is enriched in short chains. In maize, potato and pea, genes for all three forms of SS exist, however, the dominant activity in maize endosperm is SSI, whereas in pea embryos it is SSII, and in potato tubers it is SSIII. It is most interesting to discover in applicants' recent studies using maize that the different SS enzymes have different catalytic capabilities to synthesize various glucan chain lengths. For example, SSI synthesizes shorter chains whereas TABLE 1 A Comparison of K_(d) values of Maize Granule Bound Starch Synthase (GBSS) and SS1-2 Temperature (° C.) 4 Room Temperature (˜23.5) Type of GBSS SSI-2 GBSS SSI-2 Glucan mM Amylose 0.14 ± 0.01 0.35 ± 0.150 ± 0.01  1.06 ± 0.12 0.07^(a) Amylo- 0.015 ± 0.001 0.06 ± 0.00 0.054 ± 0.004 0.07 ± 0.03 pectin Glycogen  1.50 ± 0.369 1.20 ± 0.03 (no binding) 3.38 ± 0.83

[0005] TABLE II Comparison of K-values of maize SSI and SSI-2, with α-amylase (porcine pancreas) and glucoamylase (Aspergillus niger) Maize SSI Maize SSI-2 α-amylase glucoamylase Substrate mg/mL mM mg/mL mM mg/mL mM mg/mL mM Starch 0.261 0.069^(a) 0.241 0.065^(a) 0.539 0.144^(a) 0.090 0.024^(a) Amylopectin 0.217 0.076 0.242 0.078 0.602 0.212 0.030 0.010

[0006] GBSS synthesizes very long chains. SSIIa and SSIIb synthesize shorter and more intermediate chains, and SSIII (DuI) synthesizes relatively long chains. Also, these enzymes differ in their glucan binding affinities. SSIIa does not bind to any given glucan of any particular chain lengths that we tested, where as SSIIb displayed partial or minor glucan affinity and SSI binds with greatest affinity to longer glucan chains in amylopectin. This observation explains why SSIIa or SSIIb enzymes are not entrapped in the starch granules and SSI does entrap during the course of starch synthesis. The present invention provides modified starch, and methods of making and using the same, by, for example, structural modification by genetic manipulation of SS enzymes, which is possible due to the presently disclosed discovery of the specificity displayed by the enzymes described herein to a given glucan chain length. This can be accomplished by several ways and listed below and described herein are a few examples: (a) regulating the expression levels of SS enzymes, (b) alteration of the starch biosynthetic pathway by incorporation of the genes encoding one or more enzymes involved in the starch or glycogen biosynthetic pathway, (c) increasing the association of SSIIa, SSIIb and Du1 with the starch granules especially, by engineering entrapment of their corresponding enzymes with the starch granules, and (d) entrapment of fusion proteins of SS enzymes, for example, catalytic domains of SSIIa, SSIIb and Du1 in association with glucan binding domains of GBSS or SSI in the starch granules to bring a change in the glucan chain lengths and distribution and thereby synthesize modified starch.

[0007] U.S. Pat. Nos. 5,824,790, 6,130,367, and 5,300,145 describe methods of (a) and (b) of the above. The international application WO 92/11376 describes a method for suppressing amylose formation in potato by transforming potato plant with a construct comprising antisense fragments designed to inhibit the expression of GBSS gene. The Canadian patent application 2,061,143 describes a similar technique for producing amylose free potato starch. The production of modified starches by plants transformed with genes encoding enzymes involved in starch synthesis is described for example in DE-A-19534759, WO 92/14827 in which branching enzyme derived from potato cDNA is used and WO 92/11376 describes an alternative method for antisense suppression of GBSS activity in plants.

[0008] However, none of these above mentioned patents describe the combination of different domains of SS enzymes, for example starch association domain (“GLASS” domain) of one enzyme, like GBSS to the catalytic domain (“GLYTR” domain) of another, for example SSIIa, in order to bring a modification to the structure of starch. Surprisingly, the applicants discovery of threading SS enzymes using 3D-PSSM (three-dimensional position-specific scoring matrix) program (Kelley et al., 2000, J. Mol. Boil. 299:499-520) to predict three dimensional structure of SS enzymes and the sequence comparisons revealed two distinct domains for each one of these enzymes (herein after referred to as “GLASS” and “GLYTR”). 3D-PSSM uses structural alignments of homologous proteins of similar three-dimensional structure in the structural classification of proteins (SCOP) database to obtain a structural equivalence of residues. These equivalences are used to extend multiply aligned sequences obtained by standard sequence searches. The resulting large-superfamily based multiple alignment is converted into a PSSM (position specific scoring matrix). Combined with secondary structure matching and solvation potentials, 3D-PSSM can recognize structural and functional relationships beyond state-of the-art sequence methods (Kelly et al., 2000, J. Mol. Biol. 299:499-520). Analysis through 3D-PSSM revealed a conserved two domain 3D structure for all maize starch synthases tested (FIG. 5). This is the first ever report in the scientific literature to model the 3D structure of any starch synthases. Using ProDom database of protein domain families available at the world widee web address Toulouse.inra.fr/prodom.html, Denyer et al., 2001; J. of Plant. Physiol. 158: 479-487, showed identity to three different domains in maize SS enzymes. However, they have not identified a function to Domain I and II and reported that Domain II is also found in Yeast α-amlyase. They reported Domain III as a putative glucosyl transferase domain, but neither provided detailed information as to which group in this family that maize SS enzymes fall under, nor sequence homology or models for 3D-structure of SS protein. Present invention provides the discovery of “GLYTR” domains for all these enzymes as a catalytic domain with significant alignments (using RPS-BLAST 2.2.2; oasis_sapv1.54 database and Domain architectural retrieval tool [DART]) to the glycosyl transferase group-1 domain otherwise referred to as the pfam00534 family (FIG. 6 & Table III). Members of this family are spread across about at least 20+ groups with different mechanism of glycosyl transferase function. Members of the pfam 00534 (PI00534) family transfer UDP, ADP, GDP or CMP linked sugars to a variety of substates including glycogen. The sequence in the catalytic or “GLYTR” domains is highly conserved in starch synthases (Table IV). Furthermore, the present invention relates to the identification of “GLucan ASSociation Domain (“GLASS” Domain), peptides and nucleic acids encoding the same. Glucan chain length specificity is conserved in “GLASS” domain of each form of starch synthase and glycosyl transferase function is conserved in “GLYTR” domain. In addition, starch entrapment function is also embedded in the “GLASS” domain of GBSS and SSI. Also, via genetic means, the present invention provides for generation of starch synthase(s) with novel functionalities by combining various domains from different synthases, i.e. by mixing and matiching functional “GLYTR” and “GLASS” domains from different organisms. Thus, the present invention in particular relates to modification to starch structure by increasing the association of SSIIa, SSIIb and Du1 with the starch granules especially, by engineering entrapment of their corresponding enzymes with the starch granules, and expression and entrapment of fusion proteins of SS enzymes, for example, catalytic domains of SSIIa, SSIIb and Du1 in association with glucan binding domains of GBSS or SSI in the starch granules to bring a change in the glucan chain lengths and distribution and thereby synthesize modified starch. The present invention provides modified plants which contain altered or modified starch synthase domains or polypeptide fusions expressed inside the amyloplast stroma and become associated with the starch granules of economically important crops like maize, potato, rice, oat, wheat, barley, sweet potato, cassaya, taro, sago, yam, banana, pea, etc. These SS enzyme fusions thus expressed will alter or influence the starch structure leading to plants with improved starch properties and modified starches with various industrial uses. Further applications and embodiments of this invention will be explained in detail herein below. TARI F III % align- ENZYME Seq. ID No. Alignment with Pfam 00534 (Glycosyl transferase, Group 1 domain) ment GBSS SEQ ID NO:11 query: 378 NKEALQAEVGLPVDRNIPLVAFIGRLEEQKGPDVMAAAIPQLME-MVEDVQIVLLGTGKK 436 91.3 (query) Sbjct: 1 DREEIRKKLGIKEEKKI--ILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGG 58 SEQ ID NO:12 Query: 437 KFERMLMSAEEKFPGKVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTP 496 (snjct) Sbjct: 59 EDELKLLALKLGLEDNVIFLGFVPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLP 118 Query: 497 CACASTGGLVDTIIEGKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIK 545 Sbjct: 119 VIATDVGGIPEIVKDGETGL----------LVEPGDVEALAEAIEKLLK 157 SSI SEQ ID NO:13 Query: 441 LPIRPDVPLIGFIGRLDYQKGID-LIQLI--IPDLMREDVQFVMLGSGDPELEDWMRSTE 497 75 (query) Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 SEQ ID NO:14- Query: 498 SIFKDKFRGWVGF-SVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGGL 556 (snjct) Sbjct: 69 LGLEDNVI-FLGFVPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGGI 127 Query: 557 RDTVENFNPFGENG 570 Sbjct: 128 PEIVKD----GETG 137 SSIIa SEQ ID NO:15 Query: 540 LEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIA---GQDVQLVMLGTGRADLERMLQHLE 596 84.3 (query) Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 SEQ ID NO:16 Query: 597 REHPNKVRGWVGFSVPMAHRIT--AGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 654 (snjct) Sbjct: 69 LGLEDNVI-FLGF-VPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGG 126 Query: 655 LRDTVAPFDPFGDAGLGWTFDRAEANKLIEALR 687 Sbjct: 127 IPEIVKDGET------GLLVEPGDVEALAEAIE 153 SSIIb SEQ ID NO:17 Query: 506 LQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIA---GQDVQLVMLGTGRADLEDMLRRFE 562 87.2 (query) Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 SEQ ID NO:18 Query: 563 SEHSDKVRAWVGFS----VPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAV 618 (snjct) Sbjct: 69 LGLEDNVI-FLGFVPDEDLPELYKS---ADVFVLPSRYEGFGIVLLEAMACGLPVIATDV 124 Query: 619 GGLRDTVAP------FDPFNDTGLGWTFDRAEAN 646 Sbjct: 125 GGIPEIVKDGETGLLVEPGDVEALAEAIEKLLKD 158 DuI SEQ ID NO:19 Query: 1478 PVVGIVTRLTAQKGIHLIKHAIHRTLERNGQVVLLGSAPDSRIQADFVNLANTLHGVNHG 1537 70.3 (query) Sbjct: 16 KIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALKLGLEDNV 75 SEQ ID NO:20 Query: 1538 QVRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTQLVAMRYGTIPIVRKTGGLFDTVFD 1597 (snjct) Sbjct: 76 IFLFGVPDEDLPEL--YKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGGIPEIVKD 133 Query: 1598 VDN 1600 Sbjct: 134 GET 136

[0009] TABLE IVa PIR Multiple Alignment for “GLYTR” Domain of Maize SS enzymes Enzyme (res. # of the SEQ ID start) NO:. CLUSTAL W (1.8) multiple sequence alignment SSIIa-540 21 -----------EVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIAG--QDVQLVMLGTG----- RADLERMLQHLEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGGLRDTVAPFDP- FGDAGLGWTFDRAEANKLIEALR--- SSIIb-506 22 ----------LQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIAG--QDVQLVMLGTG----- RADLEDMLRRFESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGGLRDTVAPFDP- FNDTGLGWTFDRAEAN---------- SSI-441 23  -------- LPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLMR--EDVQFVMLGSG----- DPELEDWMRSTESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGGLRDTVENFNP- FGENG--------------------- GBSS-378 24 NKEALQAEVGLPVDRNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTG----- KKKFERMLMSAEEKFPGKVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIEGKTGFHMGR LSVDCNVVEPADVKKVATTLQ Du1-1478 25 -----------------PVVGIVTRLTAQKGIHLIKHAIHRTLE--RNGQVVLLGSAPDS RIQADFVNLANTLHGVNHGQVRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTQLVAMR YGTIPIVRKTGGLFDTVFDVDN--------------------------                  *::.:: **  *** .::   :       .:*.*:**:.        .:       .    .:.*  : :. .::* * **.*.: :.* ****** ** .*  ***      .*** **:   .

[0010] TABLE IVb PIR Multiple Alignment of SSI and SSII enzymes ENZYME CLUSTAL W (1.8) multiple sequence alignment SEQ ID NO: SSIIA.     MSSAAVSSSSSTFFLALASASPGGRRRARVGSSP---FHTGASLSFAFWAPPSPPRAPRD 26 SSIIB.     -MPGAISSSSSAFLLPVASSSPR-RRRGSVGAALRSYGYSGAELR-LHWARRGPPQD--G 27 SSI. --MATPSAVGAACLLLARAAWP-----AAVG-----------DR-----ARPRRLQR--- 29         .: *: .:: :*   :: *     , **           .      *     : SSIIA.     AALVRAEAEAGGKDAPPERSGDAARLPRARRNAVSKRRDPLQPVGRYGSATGNTARTGAA 26 (cont.d) SSIIB.     AASVRAAAAPAGGESEEAAKSSSSSQAGAVQGSTAKAVDSASPPNPLTSAP---KQSQSA 27 SSI. -VLRRRCVAELSREGPAPRPLPPALLA------P-----PLVP----------------- 29       .  *  .   . :.       .:  .            .  * SSIIA.     SCQNAALADVEIKSIVAAPPTSIVKFPAPGYRMILPSGDIAPETVLPAPKPLHESPAVDG 26 (cont.d) SSIIB.     AMQNG------------------------------TSGGSSASTAAPVSGPKADHPSAPV 27 SSI. -------------------------------------G-FLAPPAEPTGEPASTPPPVP- 29                                          *   . .. *.  *    *.. SSIIA.     DSNGIAPPTVEPLVQEATWDFKKYIGFDEPDEAKDDSRVGADDAGSFEHYG-DNDSGPLA 26 (cont.d) SSIIB.     TKREIDASAVKPEPAGDDARPVESIGIAEPVDAKADAAPATDAAASAPYDREDNEPGPLA 27 SSI. -DAGLGDLGLEPE------------GIAEG--SIDNTVVVASEQDSEIVVGKEQARAKVT 29       .  :    ::*             *: *   :  ::   :.   *      ::  . :: SSIIA.     GENVMNVIVVAAECSPWCKTGGLGDVVGALPKALARRGHRVMVVVPRYG------DYVEA 26 (cont.d) SSIIB.     GPNVMNVVVVASECAPFCKTGGLGDVVGALPKALARRGHRVMVVIPRYG------EYAEA 27 SSI. ----QSIVFVTGEASPYAKSGGLGDVCGSLPVALAARGHRVMVVMPRYLNGTSDKNYANA 29           .::.*:.*.:*:.*:****** *:** *** ********:***       :*.:* SSIIA.     FDMGIRKYYKAAGQDLEVNYFHAFIDGVDFVFIDAPLFRHRQDDIYG---GSRQEIMKRM SSIIB.     RDLGVRRRYKVAGQDSEVTYFHSYIDGVDFVFVEAPPFRHRHNNIYG---GERLDILKRM SSI. FYTEKHIRIPCFGGEHEVTFFHEYRDSVDWVFVDHPSY-HRPGNLYGDKFGAFGDNQFRY           :      * : **.:** : *.**:**:: * : ** .::**   *   :   * SSIIA.     ILFCKVAVEVPWHVPCGGVCYGDGNLVFIANDWHTALLPVYLKAYYRDHGLMQYTRSVLV 26 (cont.d) SSIIB.     ILFCKAAVEVPWYAPCGGTVYGDGNLVFIANDWHTALLPVYLKAYYRDNGLMQYARSVLV 27 SSI. TLLCYAACEAPLILELGGYIYG-QNCMFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILV 29       *:* .* *.*     **  **  * :*:.****::*:** * * **  *: : :**:** SSIIA.     IHNIAHQGRGPVDEFPYMDLP-------EHYLQHFELYDPVG-GEHANIFAAGLKMADRV 26 (cont.d) SSIIB.     IHNIABQGRGPVDDFVNFDLP-------EHYIDHFKLYDNIG-GDHSNVFAAGLKTADRV 27 SSI. IHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHALDKGEAVNFLKGAVVTADRI 29      ***:****  *.. :  :.**       *  : .:   . :. *:  *.: ..:  ***: SSIIA. LETLDAGKRQCKAALQRELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIAGQDVQLV 26 (cont.d) SSIIB. FETLDTGKRQCKAALQRQLGLQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIAGQDVQLV 27 SSI. VDDLS-GKAKCKGALQKELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLMREDVQFV 29  : *. ** :**.***::*** .* ****:******* ***:*:*   :  :  :***:*          MLGTGRADLERMLQHLEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLY 26 (cont.d) SSIIA.          MLGTGRADLEDMLRRFESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLY 27 SSIIB.          MLGSGDPELEDWMRSTESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLY 29 SSI.          ***:* .:**  ::  *  . *.*. *******::*******.*::************** SSIIA.          AMAYGTVPVVHAVGGLRDTVAPFDPFGDAG--- 26 (cont.d) SSIIB. LGWTFDRAEANKLIEALRHCLDTYRKY 27 SSI.          AMAYGTVPVVHAVGGLRDTVAPFDPFNDTG--- 29 LGWTFDRAEANRMIDALSHCLTTYRNY          AMQYGTVPVVHATGGLRDTVENFNPFGENGEQGTGWAFAPLTTENMFVDIANCN-----     -          ** *********.*******  *:**.: *    **:*    ::.::  : :* SSIIA.     GESWKSLQARGMSQDLSWDHAAELYEDVLVKAKYQW 26 (cont.d) SSIIB.     KESWRACRARGMAEDLSWDHAAVLYEDVLVKAKYQW 27 SSI. ------IYIQGTQVLLGRANEARHVKRLHVGPCR-- 29

[0011] TABLE V Possible, but not limited to Amino acid Sequences for Some of the Proposed Fusion Proteins A GBSS(61-300) + Du1 (1201-1674) RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS SEQ ID NO:30 VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN WMKAGILEAD RVLTVSPYYA EELISGIARG CELDNIMRLT GITGIVNGMD VSEWDPSRDK GGIYDNRNGL DYHIPVFGSI AKEPPMHIVH IAVEMAPIAK VGGLGDVVTS LSRAVQDLGH NVEVILPKYG CLNLSNVKNL QIHQSFSWGG SEINVWRGLV EGLCVYFLEP QNGMFGVGYV YGRDDDRRFG FFCRSALEFL LQSGSSPNII HCHDWSSAPV AWLHKENYAK SSLANARVVF TIHNLEFGAH HIGKAMRYCD KATTVSNTYS KEVSGHGAIV PHLGKFYGIL NGIDPDIWDP YNDNFIPVHY TCENVVEGKR AAKRALQQKF GLQQIDVPVV GIVTRLTAQK GIHLIKHAIH RTLERNGQVV LLGSAPDSRI QADFVNLANT LHGVNHGQVR LSLTYDEPLS HLIYAGSDFI LVPSIFEPCG LTQLVAMRYG TIPIVRKTGG LFDTVFDVDN DKERARDRGL EPNGFSFDGA DSNGVDYALN RAISAWFDAR SWFHSLCKRV MEQDWSWNRP ALDYIELYRS ASKL B. GBSS (61-300) + 551 (400-622) RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS SEQ ID NO:31 VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN KATTVSNTYS KEVSGHGAIV PHLGKFYGIL NGIDPDIWDP NGIDINDWNP ATDKCIPCHY SVDDLSGKAK CKGALQKELG LPIRPDVPLI GFIGRLDYQK GIDLIQLIIP DLMREDVQFV MLGSGDPELE DWMRSTESIF KDKFRGWVGF SVPVSHRITA GCDILLMPSR FEPCGLNQLY AMQYGTVPVV HATGGLRDTV ENFNPFGENG EQGTGWAFAP LTTENMFVDI ANCNIYIQGT QVLLGRANEA RHVKRLHVGP CR C. GBSS (61-300) + SSIIa (481-732) RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS SEQ ID NO:32 VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN DIIRSNDWKI NGIVNGIDHQ EWNPKVDVHL RSDGYTNYSL ETLDAGKRQC KAALQRELGL EVRDDVPLLG FIGRLDGQKG VDIIGDAMPW IAGQDVQLVM LGTGRADLER MLQHLEREHP NKVRGWVGFS VPMAHRITAG ADVLVMPSRF EPCGLNQLYA MAYGTVPVVH AVGGLRDTVA PFDPFGDAGL GWTFDRAEAN KLIEALRHCL DTYRKYGESW KSLQARGMSQ DLSWDHAAEL YEDVLVKAKY QW D. GBSS (61-300) + SSIIb (481-698) RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS SEQ ID NO:33 VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN YTNYTFETLD TGKRQCKAAL QRQLGLQVRD DVPLIGFIGR LDHQKGVDII ADAIHWIAGQ DVQLVMLGTG RADLEDMLRR FESENSDKVR AWVGFSVPLA HRITAGADIL LMPSRFEPCG LNQLYAMAYG TVPVVHAVGG LRDTVAPFDP FNDTGLGWTF DRAEANRMID ALSHCLTTYR NYKESWRACR ARGMAEDLSW DHAAVLYEDV LVKAKYQW

SUMMARY OF THE INVENTION

[0012] The invention provides the polypeptide sequence of GBSS enzymes (FIGS. 9A & 9B) that will enable the fused polypeptides of other starch synthases to become entrapped in the starch granules and be functional. The present invention provides modified starches with altered glucan chain lengths and a variety of starch synthase polypeptide domain fusions (TABLE V) to produce the same, as well as gene constructs that encode such fusions and in methods for the transformation of plants using such constructs as well as in the transformed plants thus obtained. The present invention also relates to the expression in plants of polypeptides-including SS enzymes as fusion proteins with improved affinity to starch and modified catalytic capabilities and to the in vivo and in vitro synthesis of glucan chains of modified lengths as compared to a plant producing native starch or starch produced with native starch synthases. In particular, the invention relates to the expression in plants of soluble starch synthase protein domains and/or polypeptide domains as fusion peptides with starch association domain of GBSS or SSI or any other SS enzyme. According to this invention, GBSS is any fusion protein thus generated using GBSS, for example, any SS or any other enzyme domain plus GLASS domains of GBSS and may include GLYTR domain as well. SS or Starch synthase means any starch synthesis enzyme that is present in soluble form, for eg. SSI, SSIIa, SSIIb, and SSIII.

[0013] The present invention provides a method for obtaining transformed plants that produce starches with modified glucan chain lengths. A farther object of this invention is to express the desired starch synthases or polypeptides in plants with modified functionalities in vivo and in association with starch or starch granules in order to introduce a desired modification in the average chain length of amylopectin.

[0014] The above objects are achieved by expressing a desired fusion protein of starch synthase or polypeptide that can interact with starch or starch granule in bringing a modification of glucan chain lengths.

[0015] By “interact with starch or starch granules” is generally meant that the fusion protein of starch synthases can modify, alter the chain length distribution of starch or modify the fine structure of starch. This interaction will result in starch or starch granules that differ from the naturally occurring plant starch in at least one property thereof, for example, glucan chain lengths, glucan composition, crystallinity, branching degree etc. Therefore, starch synthase fusion protein will influence at least one physical or chemical property of the starch.

[0016] Broadly, the invention relates to a method for expressing fusion proteins consisting of a desired one or more catalytic domains (“GLYTR” Domain) of one or more starch synthase or any other enzyme in association with glucan association domain (“GLASS” Domain) of GBSS or similar enzyme.

[0017] In addition, the invention also relates to a method for expressing fusion proteins consisting of a desired one or more catalytic domains (“GLYTR” Domain) of one or more starch synthase or any other enzyme in association with glucan association domain (“GLASS” Domain) of SSI or other similar enzymes.

[0018] The invention also relates to a method for expressing fusion proteins consisting of a desired domain (“GLASS” Domain) of any starch synthase enzyme from any organism fused with another desired domain of another starch synthase enzyme (“GLYTR” Domain) from the same or any other organism in any combination and vice versa.

[0019] The starch synthase protein domains or polypeptides expressed via the method of invention can be from any plant or from any plant part including seeds, leaves, roots, tubers, stems, stalks, fruits, and/or flowers. The starch synthase polypeptides thus expressed may or may not by themselves have natural affinity for starch or starch granules, and the method of the invention is used to provide a polypeptide of GBSS or SSI with such affinity.

[0020] Furthermore, the starch synthase polypeptides thus expressed may not by themselves have the natural affinity for starch or starch granules, and the method of invention is used to provide a polypeptide of SSI with such affinity.

[0021] The transformants of the invention expressing the starch synthase fusion proteins, may change the starch structure in different forms. For example, the starch synthases of the invention can change any one or the more of crystallinity of said starch, can change the glucan content, degree of branching, and especially the length of glucan chains in the amylopectin molecule.

[0022] The above modification in the glucan chain length distribution can bring changes in the affinity of the starch synthase enzymes that are intrinsic to the starch granule. And the change can increase or decrease the association of intrinsic starch synthase enzymes, like SSI and GBSS, to the starch granules.

[0023] Therefore, a further aspect of the invention relates to a method for providing a recombinant protein or polypeptide with affinity for starch granules and that has catalytic activity in order to bring changes in the structure of the starch.

[0024] The genes encoding the desired starch synthase polypeptide sequence may be derived from any source, including plants, animals, fungi, algae, yeasts, bacteria, and any other microorganisms. The expressed genes may be homologous or heterologous to the starch producing plant in which the fusion peptides of starch synthase are expressed.

[0025] A further aspect of the invention is that the genes encoding any of the starch synthase fusion polypeptides can be variants or mutants of such proteins, such as those known in the art and/or obtainable via genetic manipulations. This includes mutant enzymes with biological activity but, with altered properties in terms of altered substrate binding activity, altered substrate specificity, and finally altered kinetic properties.

[0026] In another aspect the present invention provides expression of fusion proteins with of the invention is that the expression of fusion proteins with the starch association domain of SSI and/or GBSS (“GLASS” Domain) which may include partial or full length catalytic domains of any starch synthases, starch branching enzymes, debranching enzymes, disproportionating enzymes, kinases, phosphorylases and any of the isoforms of above enzymes.

[0027] More in particular, the expression of these starch synthase fusion proteins along with the starch association domain of GBSS will lead to a “modified-starch”, the subject matter of invention.

[0028] The said modified starch may be further modified according to the techniques known to the skilled person. Whether in modified or unmodified form, the starch will be used for food and non-foodstuff.

[0029] The above “modified starch” resulting from the expression of fusion proteins of starch synthases will have at least one of the listed below altered or improved properties as compared to the natively produced starch by a plant. The modified starch will have an altered or improved morphology, retrogradation, waterbinding or swelling potential of the granules, gel strength, adhesiveness, cohesiveness, hardness, elasticity, increased or decreased granule size, degree of branching, crystallinity, degree of cross-linking, and increased or decreased glucan chain lengths.

[0030] The present invention further provides the following method of:

[0031] a) providing a genetic construct containing at least one or more nucleotide sequence encoding desired polypeptide sequence containing one or more catalytic domains (“GLYTR” Domain) of starch synthase fusion protein combined with at least one nucleotide sequence encoding starch association domain (“GLASS” Domain) of GBSS or SSI;

[0032] b) providing a genetic construct containing at least one or more nucleotide sequence encoding desired polypeptide sequence(s) containing at least one domain (“GLYTR”or “GLASS” Domain) of one starch synthase with at least one nucleotide sequence encoding desired polypeptide sequence of another domain (“GLYTR”or “GLASS” Domain) of another starch synthase and vice versa;

[0033] c) transforming a plant with any of the above construct(s); and

[0034] d) expressing the genetic construct in the plant in vivo.

[0035] The present invention provides an isolated DNA molecule encoding a fusion protein consisting of four different functional domains selected from the group consisting of GLASS, LINKR, GLYTR, and CTEND which are operably linked to one another. The isolated DNA molecule of the present invention may contain, for example, a GLASS domain which contains a GBSS GLASS. Further, the GBSS GLASS of the present invention may contain a GLASS of SEQ ID NO: 1. Alternatively, the isolated DNA molecule of the present invention may contain a GLASS domain which contains a SSI GLASS. The SSI GLASS of the present invention may contain, for example, a GLASS of SEQ ID NO: 2. Moreover, the isolated DNA molecule of the present invention may contain a GLASS domain which contains a SSII GLASS. For example, the SSII GLASS of the present invention may ontain a GLASS of SEQ ID NOs: 3 and/or 4. Furthermore, the isolated DNA molecule of the present invention may contain a GLASS domain which contains a SSIII GLASS. The SSIII GLASS of the present invention may further contain a GLASS of SEQ ID NO:5

[0036] In one embodiment, the isolated DNA molecule of the present invention contains at least one of a GBSS GLASS, a SSI-GLASS, a SSII-GLASS or a SSII-GLASS wherein the GLASS or GLASS domain are a GLASS or GLASS domain of a glucan producing organism or at least 80% (preferably at least 85%, more preferably at least 90%, alternatively at least 95%, or at least 98%) identical or similar to a GLASS or GLASS domain peptide of a glucan producing organism.

[0037] The present invention further provides an isolated DNA molecule, as described herein and above wherein the LINKR domain is a GBSS-LINKR, a SSI-LINKR, a SSII-LINKR and/or a SSIII-LINKR. The LINKR of the invention may contain a LINKR sequence containing any of SEQ ID NOs:121-171; 336-386;527-577; 733-783; and/or 983-1033.

[0038] The present invention further provides an isolated DNA molecule, as described herein wherein the GLYTR domain may contain a GBSS-GLYTR, a SSI-GLYTR, a SSII-GLYTR and/or a SSIII-GLYTR. More specifically, the GLYTR domain of the present invention may contain a GLYTR sequence containing at least one of SEQ ID NOs:1136, 1137, 1138, 1139, and/or 1140. Alternatively, the GLYTR of the present invention may contain a GLYTR sequence containing at least one of SEQ ID NOs: 172-222; 387-437; 578-628; 784-834; and/or 1034-1084.

[0039] The present invention further provides an isolated DNA molecule, as described herein and above wherein the CTEND domain is a GBSS-CTEND, a SSI-CTEND, a SSII-CTEND and/or a SSIII-CTEND. The CTEND of the invention may contain a CTEND sequence containing any of SEQ ID NOs: 1146, 1147, 1148, 1148, 1149 and/or 1150. Alternatively, the CTEND of the present invention may contain a CTEND sequence containing a CTEND sequence containing at least one of SEQ ID NOs:223-266; 438-461; 629-676; 835-882; and/or 1085-1135.

[0040] The present invention provides an isolated DNA molecule encoding a fusion peptide which contains a GBSS GLASS domain operably linked to a LINKR and a catalytic domain from a functional protein that synthesizes an ∀-1,4 glucan or an ∀-1,3 glucan, or an ∀-1,6 glucan, wherein the fusion peptide is capable of modifying the glucan structure of a starch producing organism when starch is produced by such an organism or part thereof in the presence of a fusion peptide of the present invention.

[0041] In a further embodiment, the present invention provides a DNA molecule which encodes a fusion peptide, and a fusion peptide coded for by the same, wherein the GLASS and/or LINKR sequence contained therein contains at least one of SEQ ID NOs:75-120; 284-335, 475-526; 682-732; 933-982 and/or 121-171, 336-386, 527-577, 733-783, and 983-1033.

[0042] In a further embodiment, the present invention provides an isolated DNA molecule encoding a polypeptide, and a polypeptide so encoded, with glucan association properties of a maize GBSS enzyme, and being capable of modification of starch metabolism in a plant or plant cell, the DNA containing a molecule of, for example, at least one of the following:

[0043] (a) a DNA molecule encoding a protein domain having the amino acid SEQ ID NO:1;

[0044] (b) a DNA molecule containing a corresponding nucleotide sequence from SEQ ID No:1141;

[0045] (c) a DNA molecule containing a nucleotide sequence differing from the sequence of the DNA molecules of (a) or (b) due to the degeneracy of the genetic code;

[0046] (d) a DNA molecule containing a DNA sequence which hybridizes to any one of the DNA molecules of (a), (b) or (c) or fragment thereof, and which is equal to or more than 80% homologous or identical or similar to the DNA molecule of (a), (b), or (c), or fragment thereof, wherein the DNA sequence encodes a polypeptide with Glucan Association Domain (Domain A) of a GBSS enzyme.

[0047] The present invention provides an isolated DNA molecule encoding a polypeptide with a glycosyl transferase function of a soluble or granule bound maize SS enzymes capable of modifying starch metabolism in a plant or plant cell, the DNA molecule containing, for example, at least one of the following:

[0048] (a) a DNA molecule encoding a protein domain containing an amino acid of SEQ ID NOs:1, 2, 3, 4, and 149;

[0049] (b) a DNA molecule containing the corresponding nucleotide sequence of SEQ ID NOs: 1141, 11142, 1143, 1144, and 1145;

[0050] (c) a DNA molecule containing a nucleotide sequence differing from the sequence of the DNA molecules of (a) or (b) due to the degeneracy of the genetic code,

[0051] (d) a DNA molecule containing a DNA sequence which hybridizes to any one of the DNA molecules of (a), (b) or (c), or fragment thereof, and which is equal to or more than 80% homologous or identical to the DNA molecule of (a), (b), or (c), or fragment thereof, wherein the DNA sequence encodes a polypeptide with a glycosyl transferase domain of a SS enzyme.

[0052] The present invention provides a recombinant or isolated DNA molecule, as described, containing a maize GBSS nucleotide coding region encoding for an amino acid sequence of SEQ ID NOs: 101-146 fused with a corresponding coding region of a maize SS enzyme that encode for an amino acid sequence containing any of SEQ ID NOs: 35-74; 121-171; 172-222; 223-266; 268-283; 284-335; 336-386; 387-437; 438-461; 463-474; 475-526; 527-577; 578-628; 629-676; 678-681; 682-732; 733-834; 835-882; 884-932; 933-982; 1034-1084; and/or 1085-1135.

[0053] The present invention provides a recombinant or isolated DNA molecule, as described, containing a GLYTR, LINKER or CTEND domain DNA sequence containing any of SEQ ID NOs: 172-222; 387-437; 578-628; 784-834; 1034-1084, 121-171; 336-386; 527-577; 733-783; 983-1033 or 223-266; 438-461; 629-676; 835-882; 1085-1135 operably linked in any order with a corresponding DNA sequence that encodes for a glucan association domain containing any of SEQ ID NOs: 75-120; 284-335; 475-526; 682-732; and/or 933-982.

[0054] The present invention provides a recombinant or isolated DNA molecule, as described, further containing a DNA sequence differing from the sequence of any of the DNA molecules of SEQ ID NOs: 34-1150 due to the degeneracy of the genetic code, and/or protein or polypeptide originating from a different source, such as a plant species other than plant species such as maize, bacteria (e.g. E. Coli), Yeast, algae (Chlamydomonas), or fungus.

[0055] The present invention provides a recombinant or isolated DNA molecule, as described herein, wherein the DNA sequence contains at least one coding region of a glucan association domain of SEQ ID NOs:75-120; 284-335; 475-526; 682-732; and/or 933-982 fused with a coding region of any glucan transferases listed in Table XXXVII.

[0056] The present invention further provides a method of expressing a starch synthase fusion proteins or polypeptides in a plant, in which the starch synthase protein or polypeptide domains are expressed as a fusion with a glucan association domain of granule bound starch synthase. Theprotein or polypeptide of the method of the invention may be heterologous with respect to the plant in which the fusion is expressed.

[0057] The present invention further provides a method, as described herein, wherein th method involves the steps of:

[0058] providing a genetic construct containing at least one nucleotide sequence encoding the desired protein domain or polypeptide domain combined with at least one nucleotide sequence encoding a glucan association domain of GBSS, so that the construct encodes a fusion of the desired protein/polypeptide and at least one glucan association domain;

[0059] transforming a plant with the genetic construct;

[0060] expressing the genetic construct in the plant.

[0061] The present invention further provides a method, as described herein, in which the protein or polypeptide or recombinant protein or recombinant polypeptide is an enzyme. Such an enzyme of the present invention may, for example, be an enzyme which is an enzyme that can interact and associate with starch or starch granules, or facilitate or be entrapped in starch or starch granules, and is capable of at least one of modifying, increasing, decreasing, altering or influencing starch structure or starch synthesis.

[0062] The present invention further provides a vector containing a DNA molecule as provided herein. The vectors of the present invention may contain, for example, a DNA molecule which is linked in the sense orientation to DNA elements ensuring transcription of a translatable RNA in a prokaryotic or an eukaryotic cell.

[0063] The present invention further provides a host cell containing a vector of the present invention.

[0064] In a further embodiment, the present invention provide a plant cell containing a DNA molecule of the present invention linked to a heterologous promoter.

[0065] The present invention further provides a plant containing a plant cell of the present invention. The plants according to the present invention may be, for example, a cereal, such as maize, rice, wheat, barley, oats, or a root crop, such as potato, sweet potato, cassaya, yam, taro, or other starch producing plant, such as peas or banana. Moreover, the plants of the present invention may contain or produce starch or starch granules in at least one of its parts, including its seeds, leaves, roots (tubers), tubers, stems, stalks, fruits, grains or flowers. Furthermore, the plants of the present invention include elements containing a homologous or heterologous promoter specific for expression of said DNA molecule in the at least one of its parts.

[0066] The present invention provides seeds from the plant of the present invention, which are preferably capable of expressing the recombinant molecule or DNA molecule of the present invention.

[0067] The present invention provides amodified starch derived from cells of a plant or plant part of the present invention.

[0068] In a further embodiment, the present invention provides a food or feed containing a modified starch of the present invention or plant or plant part of the present invention.

BRIEF DESCRIPTION OF THE FIGURES

[0069]FIG. 1. Shows ¹⁴C-ADPG incorporation as dpms (disintegrations per minute) into different glucan chain lengths separated on Sepharose CL-6B Column by various starch synthase enzymes from maize. The glucan (potato amylopectin and glycogen) was debranched after SS enzyme reaction and prior to running on the column. Shown in the order (from top to bottom of the figure) are, GBSS (granule bound starch synthase), Du-1 (SSIII), soluble starch synthase IIa, soluble starch synthase IIb (IIb), and soluble starch synthase I (SSI). Dp=degree of polymerization or number of glucose units. There is a significant difference in the chain length specificity of various enzymes. For example, GBSS incorporated most of the ¹⁴C-ADPG into very long glucan chains that are more than 30 units long. Du-I or SSIII incorporated more than half the label into glucan chains that are in between dp 20 and 30. SSIIa and SSIIb incorporated most of the ¹⁴C-ADPG into glucan chains that are shorter than 20. Most of the ¹⁴C-ADPG incorporation by SSI was into the glucan chains that are shorter than dp 10. Therefore, there are four distinct classes of starch synthases with differences in chain length specificity that are detected in maize endosperm.

[0070]FIG. 2. Shows results from Sepharose CL-6B chromatography of debranched products of GBSS and SSI. The figure displays clear distinction in the chain length specificities of GBSS and SSI enzymes in that ¹⁴C-labeled products of GBSS elute much earlier than the ¹⁴C labeled products of SSI. This means that GBSS elongates longer glucan chains, where as SSI elongates shorter glucan chains.

[0071]FIG. 3. Shows results from thin layer chromatography of debranched glycogen after ¹⁴C-ADPG incorporation into various glucan chains by different starch synthase enzymes in maize. Panel on the left shows the carbohydrate staining and panel on the right shows ¹⁴C-label incorporation into different glucan chain lengths. Carbohydrate staining shows that there is equal amount of carbohydrate loaded in each well. Also, there is equal amount of carbohydrate visible in each glucan class. However, panel on the right shows that each enzyme picked a different glucan class for ¹⁴C-ADPG incorporation. The numbers on the left indicate the size of the glucan in each class. Maltooligosaccharide (MOS) ladder (of known sizes) as a marker was run in order to enable us to estimate the glucan chains in each lane. The numbers 1-7 on the left panel indicate the number of glucoses. The numbers on the far left indicate the glucan chain (8-13) lengths interpreted based on the MOS ladder. The right panel shows that GBSS and Du-1 incorporated ¹⁴C-ADPG mostly into glucan chains longer than dp 13. Contrarily, SSI incorporated most of the ¹⁴C-ADPG into glucan chains that are dp 8 or 9. SSIIa incorporated most of the ¹⁴C-ADPG into glucan chains that are dp 8. SSIIb incorporated most of the ¹⁴C-ADPG label into glucan chains that are dp 11 and 12. Therefore, there appears to be a chain length specificity for each SS enzyme.

[0072]FIG. 4. Shows SDS-Page of proteins associated with the starch granules of maize kernels. Proteins from starch granules were extracted by boiling and ran on 10% polyacrylamide gels. Proteins were stained with coomassie blue. The figure shows that majority of the protein entrapped in the starch granules is GBSS and there is some SSI and branching enzymes as well.

[0073]FIG. 5. Shows proposed model for starch synthases based on 3D-PSSM automated fold recognition technique (Kelley et al., 2000). All the five known starch synthases from maize have two distinct domains with a linker in between. The labels on the top show the corresponding names of these domains based on the functionality disclosed in the present application. “GLASS” stands for glucan association domain and “GLYTR” stands for glycosyl transferase domain. “GLASS” and “GLYTR” are linked to each other by “LINKR” sequence.

[0074] GBSS is shown in FIGS. 5A-1, upper left panels.

[0075] SS1 is shown in FIGS. 5A-2, upper right panels.

[0076] SSIIa is shown in FIGS. 5A-3, lower left panels.

[0077] SSIIb is shown in FIGS. 5A-4, lower right panels.

[0078] DU1 is shown in FIGS. 5B-1 (FIG. 5. Cont.d).

[0079]FIG. 6. Is a cartoon showing the location of Glycosyl transferase group 1(Pfam 00534) domain of maize starch synthases.

[0080]FIG. 7. Shows a picture of affinity gel electrophoresis to determine glucan association peptide of GBSS.

[0081] Panel 1=Native gel containing 0.2% potato amylopectin. It shows GBSS has strong affinity to amylopectin.

[0082] Panel 2=GBSS enzyme was digested into various peptides using Endo-Glu-C or V8 enzyme. The peptides were separated on 10% SDS-PAGE gels and visualized by using silver staining of peptides.

[0083] Panel 3=Purified GBSS enzyme on 10% SDS-PAGE gels.

[0084] Panel 4=V8 enzyme peptides that were bound to amylopectin in the native gels were excised and ran on 10% SDS-gels. The arrows indicate the peptides that had affinity to glucan.

[0085] Panel 5=A renaturing gel for detecting the activity of SS enzymes. The smallest peptide from FIG. 4 of the above was blotted onto PVDF membrane. The amino acid sequence of the peptide is as follow. KIYGPVAGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWHTGPLSCYLKSNYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGYEKPVEGRKINWMKAGILEAD RVLTVSPYYA EE

[0086]FIG. 8 shows the effect of increasing avg. OCL of glycogen on the affinity (1/Kd) (graphs, A, B, C) and catalytic activity (graph D) of the SSI-2 enzyme.

[0087]FIG. 8A shows the effect of increasing avg. OCL of glycogen on the affinity (1/Kd);

[0088]FIG. 8B shows the effect of increasing avg. OCL of glycogen on the affinity (1/Kd);

[0089]FIG. 8C shows the effect of increasing avg. OCL of glycogen on the affinity (l/Kd); and

[0090]FIG. 8D shows the catalytic activity of the SSI-2 enzyme. The graphs shows increased affinity and decreased enzyme activity with increase in the average outer chain length of the substrate molecule. Graph 3B (8B) shows how the affinities of amylose, amylopectin and starch fall within the same range of modified glycogens with extended OCL and also shows upward trend in affinity after dp of about 17. Graph 3D (8D) shows the contrasting results with the enzyme activity using modified glycogens with extended OCLs. Data are average of three separate replications±SE.

[0091]FIG. 9. Shows a comparison of mobility of SSI and SSI-2 proteins in the substrate containing native gels.

[0092]FIG. 9A.

[0093] SSI and SSI-2 proteins were run in the native gels containing either none (panels 1 and 2) or 2% starch (panels 3 and 4), or 2% glycogen (panels 5 and 6). The gels were stained for activity using I2 solution (for details, see materials and methods section). The arrows indicate the binding of protein to the substrate in the gels containing 2% starch.

[0094]FIG. 9B.

[0095] Panels 2A, 2B, and 2C are coomassie staining, and panels 3A, 3B, and 3C are activity staining of the above proteins. Panels 2A, 2B, 3A, and 3B are native gels containing 2% starch and panels 2C and 3C are renaturing gels (see materials and method section for details). The gels show V8 peptide(s) of SSI (2A, 3A, 2C, and 3C) and SSI-2 (2B, 3B, 2C and 3C) that were bound to the substrate in the native gels (2A, 3A, 2C), and were active (2B, 3B, 3C). The arrows indicate the protein or peptide(s) bound to the substrate in the gels right in the well itself. For panels, 2C and 3C, molecular weight markers were shown on the left in kD.

[0096]FIG. 10. Shows a comparison of the elution profile of ¹⁴C-labeled glucans on Sepharose CL-4B column.

[0097]FIG. 10A shows debranched products of SSI reaction using unmodified glycogen.

[0098]FIG. 10B shows the results with modified glycogen (OCL=14-15).

[0099] Both were run on a Sepharose CL-4B. At the end of the enzyme reaction, carbohydrate was subjected to Isoamylase digestion (as described in the materials and methods section). Open squares are elution of total carbohydrate as absorbance at 490 nm of fractions mixed with phenol and H₂SO₄; open triangles are the elution profile of ¹⁴C-labeled products. The scale bar for each graph shows profile of elution of corresponding chain lengths of debranched amylopectin ran on the same column. Each data point is an average of 3 separate runs on the columns.

[0100]FIG. 11.

[0101]FIG. 11A shows increased affinity and increased enzyme activity of GBSS with increase in the average outer chain length of the substrate molecule.

[0102]FIG. 11B shows the contrasting results with the enzyme activities of GBSS and SSI enzyme using modified glycogens with extended OCLs. Data are average of three separate replications±SE.

[0103]FIG. 12. Shows a comparison of the glucan binding affinities of SSIIa, SS1-2, and GBSS enzymes. Affinity is calculated based on the molar availability of outer chain lengths.

[0104]FIG. 12A shows increase in the affinity of GBSS and SSI-2 enzymes to increase in the outer chain length of modified glycogen up to dp ˜14 to 16. To the same increase in the outer chain lengths, SSIIa did not show any increase in the affinity.

[0105]FIG. 12B shows a linear increase in the affinity of GBSS to further increments in the chain length whereas, SSIIa did not show any increase in the affinity.

[0106] It is interesting to note that SSI-2 displayed more than 4000 fold increase in the affinity when the length of the outer chains was extended on an average up to 21glucose units.

[0107]FIG. 13. Shows summary of activities of SSI, SSIIa, SSIIb, SSIII (DuI) and GBSS using chain extended glycogen. Based on the observations in this figure, the present invention classifies maize a-1,4 glucan transferases or starch synthases based on their specificities to process various lengths of glucan chains in the amylopectin cluster. For example, according to the present invention, ‘Class I’ enzymes that include maize SSI and like enzymes, and preferentially elongate a-1,4 glucan chains to synthesize shorter A and BI chains; ‘Class II’ enzymes that include maize SSIIa and SSIIb and like enzymes, and preferentially add a glucose unit(s) to a-1,4 glucan chains to synthesize longer A and B 1 chains and intermediate B2 or B3 chains; ‘Class III’ enzymes that include maize SSIII and GBSS, and preferentially add a glucose unit(s) to a-1,4 glucan chains to synthesize longer A, B 1, B2 and B3 chains as well as longer B3 or C chains of amylopectin. In maize or any other crop when transformed to express or over express any one specific class of starch synthases described above will result in an increased number of glucan chains in that specific class.

[0108]FIG. 13A shown A similarity in Chain Length Specificities of Du-1 and SSIIa;

[0109]FIG. 13B shows A Comparison of Chain Length Specificities of SSI-2 and SSIIb;

[0110]FIG. 13C shows A Comparison of Contrasting Catalytic Activities of GBSS and SSI to Increasing Gluican Chain Lenghs of Glycogen.

[0111]FIG. 14.

[0112]FIG. 14A shows detection of the expression of fusion proteins in the soluble extracts of transgenic maize kernels. The transgenic proteins are expressed in the soluble extracts.

[0113]FIG. 14B shows detection of the transgenic fusion protein only in the 210 and 218 (See example number I for details).

[0114]FIG. 15.

[0115]FIG. 15A shows the detection of transgenic citrate synthase protein in the soluble extracts of maize kernels. However, the protein did not get associated with the starch granules.

[0116]FIG. 15B shows activities of citrate synthase from transgenic maize kernels.

[0117]FIG. 15C (right panel) shows Western blotting of Transgenic Starch-granule proteins using GFP antibody.

[0118]FIG. 16. Shows the differences in the models generated by 3D-PSSM for different proteins. Glycogen phosphorylase from E. Coli folds very differently as compared to SS enzymes and epimerase. It confirms that all SS enzymes have a similar 2 domain but functionally different 3D structures.

[0119]FIG. 16A shows UDP-N-Acetylglucosamine 2-epimer;

[0120]FIG. 16B shows T4 phage B-glycosyltransferase;

[0121]FIG. 16C shows Glycogen phosphorylase from E. coli.;

[0122]FIG. 16D shows how the catalytic or GLYTR domains of SS enzymes fold very similar to pfam 00534 structure. FIG. 16D also shows how the glucans or glucan chains are held within the groove.

[0123]FIG. 17. Shows 3D structures of some of the proposed fusion proteins.

[0124]FIG. 17A (upper left) shown GBSS+SSIIA;

[0125]FIG. 17B (upper right) shows GBSS+SSIIB;

[0126]FIG. 17C (lower left) shows GBSS+SSI; and

[0127]FIG. 17D (loer right) shows GBSS+DuI.

[0128]FIG. 18. Shows SDS-electrophoresis and coomassie staining of proteins from various plants, namely banana fruit, basella leaf, carrot root, maize endosperm, green bean pods, rice endosperm, rutabaga root, sweet potato root, and wheat endosperm. The proteins were run on native gel containing 2% boiled starch. The peptides or proteins that were bound to the glucan in the well were visualized by coomassie staining; were excised out of the native gel, and run on 10% SDS-gel. Very few peptides were bound to the glucan (data not shown). The proteins that were bound were transferred onto a nitrocellulose membrane for performing western blotting using maize SSI antibody. There was one protein in banana, two in basella, one in carrot, two or more in maize, one or two in green beans, two in rice, none in rutabaga and two in sweet potato, and two or three in wheat, were recognized by maize SSI antibody (Figure B). In order to confirm that these proteins that were bound to the glucan in the native gel and cross-reacted with maize SSI antibody posses starch synthase activity, a renaturing gel was run (see experimental procedures for details). These gels revealed both synthetic and degradative enzyme activity (Figure C). There were two proteins in banana, two in basella, one in maize, and two in wheat that possessed synthetic activity. Degradative enzyme activity was revealed in carrot, green bean, sweet potato and wheat (C). Figure D shows mobility of starch synthase enzymes of Basella alba in native gels containing no substrates (Controls).

[0129]FIG. 18A shows SDS Gel Electrophoresis;

[0130]FIG. 18B shows Western Blot Using Maize SSI antibody;

[0131]FIG. 18C shows Gel Electrophoresis to Detect Enzyme Activities; and

[0132]FIG. 18D shows Native gel Electrophoresis of Basella leaf extracts to detect SS enzyme like activity.

[0133]FIG. 19. Shows a native gel containing 0.05% potato amylopectin and displays the differences in the mobility revealed by activity staining of maize SSI, GBSS (purified from the granules) and SSIIa enzymes.

DETAILED DESCRIPTION OF THE INVENTION

[0134] Starch is deposited in granular storage bodies in most higher plants and is composed of amylose and amylopectin. Amylose is a lightly branched glucan polymer without any specific higher order of complexity. Amylopectin is composed of glucan chains arranged in a repeating structure which is made up of a highly branched amylopectin backbone arranged with the branches primarily located in an amorphous region, followed by a highly ordered crystalline lamella region lacking in branches. This crystalline region has been represented in models as a “side chain liquid crystal”, where it's mobility state is determined by the degree of order amongst the liquid crystals. Changing the degree of order then has the effect of changing the cooking properties of the starch. In normal starches there is already known to be considerable order in these liquid crystalline lamella regions, but due to this invention this order can be increased further or even decreased. It is generally known that after degrading-away the highly branched region, the remaining glucans are found to vary in chain length quite considerably. This variation in chain length is one factor determining the degree of order in the lamella region. By increasing or reducing this variation in chain lengths, useful improvements in the properties of amylopectin inside the starch granule as well as its properties after being denatured. In another aspect of this invention is increasing the efficiency of synthesis of amylose. Thus it is possible to significantly change the properties of amylopectin and amylose with consequent changes in uses of different starches. These changes in starch properties can be characterised using various Theological instruments. A further embodiment of this invention is to increase the amount of starch formed within the developing granule as a result of a more tightly ordered array of liquid crystals. In this instance the amylopectin chains which vary in chain length are made more uniform and this has the effect in making the starch pack more densely into the same space in the liquid crystal lamellae region. This has the potential not only to change starch properties, but also to increase yield as well as to increase the density of individual starch granules. This is useful because it will increase yield and also facilitate easier isolation and purification of the new starch.

[0135] Some previously well characterized ways of altering amylose and amylopectin chain length distribution involves using mutants and/or biotechnology to alter the ratios of enzymes responsible for synthesizing starch. These enzymes include the various isoforms of starch synthases, branching enzymes and debranching enzymes. This patent envisions ways of further altering amylose and amylopectin structure by engineering changes in starch synthase proteins. In particular, specific regions of certain proteins will be linked to other regions from different proteins. This engineering is made possible by the present invention which provides the specific functions of certain domains within the starch synthase proteins. Using a combination of biochemical studies and molecular evaluation, four different regions were identified within the starch synthase class of proteins. Each domain has a different yet specific function and each function is different between the different starch synthase isoforms. First is a glucan association domain (GLASS) which is responsible for determining the chain length specificity of the enzymes and their ability to associate with starch. Second is a linker domain (LINKR) responsible for proper substrate processing and separate GLYTR and GLASS domains This domain also facilitates in setting the limits on the length of glucan chains being made. Third is a glucosyl transferase domain (GLYTR) responsible for the stepwise addition of a catalytically-activated glycosyl moiety to the non-reducing end of the amylose or amylopectin glucan chain. Fourth is the C-terminal end (CTEND),which is responsible for proper folding of the overall protein. The present invention provides, in certain embodiments, proteins, peptides and/or polypeptides which are a mix and/or match these four different domains selected from different starch synthase proteins. Since many of these proteins have been identified and cloned it is possible to envision many ways to bioengineer many different combinations of new enzymes. Such new combinations of enzymes will have significantly new properties such as increased enzyme catalytic efficiency as well as changed specificity with respect to glucan chain length. A further extension of this invention is to replace the alpha-1,4glycosyl transferase catalytic domain (GLYTR) with another glycosyl transferase domain having different properties such that the glucan addition would be in a different 3314 configuration in the amylopectin molecule. For example this enhancement could place alpha-1,3 glucans in amongst the alpha-1.4 glucans normally found in starch.

[0136] To achieve these changes in amylopectin structure and hence the properties of the starch, it is necessary to create new genes encoding these novel starch synthesizing enzymes. By bioengineering each domain from a specific target enzyme, it is possible to form a fusion protein containing each of these four domains. The domains have to placed in a specific order from N-terminus through to the C-terminal end (for example: GLASS, LINKR, GLYTR, CTEND). Next the new genes are engineered so that they are expressed in the plant. The enzymes are expressed during starch formation and have to be engineered to contain a transit peptide sequence. This will ensure correct targetting of the proteins to the amyloplast where starch is synthesised. Using biotechnological techniques well known in the art, the starch enhancement envisioned herein can be done in any organism and more particularly any organism that stores or synthesizes starch.

[0137] I. Fusion Peptides of Starch Synthases

[0138] Fusion proteins, also called “hybrid proteins” are polypeptide chains that contain of two or more proteins fused together into a single polypeptide. U.S. Pat. Nos. 5,202,247 and 5,137,819 describe hybrid proteins having polysaccharide binding domains and methods and compositions for preparation of hybrid proteins capable of binding to polysaccharide matrix. Also, U.S. Pat. No. 5,202,247 describes a hybrid protein linking a cellulase-binding region to a peptide of interest. A number of patents have outlined improvements in methods of making hybrid peptides or specific hybrid peptides targeted for specific uses. For example, U.S. Pat. No. 5,635,599 reports a circularly permuted ligand with high specificity and good binding affinity as part of the hybrid peptide. U.S. Pat. No. 5,648,244 describes a method for producing a hybrid peptide with a carrier peptide. This nucleic acid region when recognized by a restriction endonuclease creates a nonpalindromic 3-base over hang that allows the vector to be cleaved.

[0139] There are reports of vectors for engineering modification in the starch pathway of plants by use of a number of starch synthesis genes in various plants. Some of these polysaccharide enzymes bind to starch, glycogen or cellulose. The U.S. Pat. No. 5,349,123 described a vector containing DNA to form glycogen biosynthetic enzymes within plant cells to introduce changes in potato starch.

[0140] The present invention provides however fusion proteins made by combining or pairing various functional polypeptide domains of starch synthases to introduce a modification in the starch structure (Table V). In the present invention, the starch association domain of GBSS enzyme is fused with the functional or catalytic domains of other various SS enzymes with different and specific functionalities to introduce modifications to starch structure.

[0141] Preferred recombinant nucleic acid molecules of this invention comprise DNA encoding the above domains (“GLYTR” or “GLASS” Domains) from any organism and comprise gene sequences set forth in the tables hereof.

[0142] Preferred plasmids of this invention are adapted for use with specific hosts. Plasmids comprising a promoter, a plastid-targeting sequence, a nucleic acid sequence encoding the above domains and a terminator sequence are provided herein. Such plasmids are suitable for insertion of DNA sequences encoding the “GLYTR”or “GLASS”domains with a LINKR or space sequence in between for expression in selected hosts. The invention includes plasmids comprising promoters adapted for both prokaryotic and eukaryotic hosts. The said promoters may also be specifically adapted for expression in monocots or in dicots.

[0143] The said fusion polypeptide according to the present invention has five regions. N-terminal GLASS LINKR GLYTR CTEND ARM_((transit peptide)) Peptide Peptide Peptide Peptide

[0144] LINKR peptide is the region between the GLASS and GLYTR and can comprise any of the sequences listed in SEQ ID NO's 243-339.

[0145] CTEND is the C-terminal region of GBSS and similar proteins and can comprise 20 to 40 amino acid residues from the list provided in Seq ID NO.I

[0146] The DNA Construct for expressing the fusion protein domains within the host, broadly is as follows: Transit Peptide/ And/or N-term Promoter ARM Termi- Coding Coding Regions for fusion peptides nator Intron* region GLASS LINKR* GLYTR CTEND*

[0147] As is known in the art, a promoter is a region of DNA controlling transcription. Different types of promoters will be selected for different hosts. Lac and T7 promoters work well in prokaryotes, the ³⁵S CaMV promoter works well in dicots. And the polyubiquitin promoter works well in many monocots. Other suitable promoters include maize 10 kDa Zein promoter, GBSS promoter, ST1 promoter, TR1 promoter, napin promoter etc. Any number of different promoters are known to the art can be used within the scope of this invention. It can be constitutive, inducible, tissue specific and may be homologous or heterologous to the said plant.

[0148] Also, as is known to the art, an intron is a nucleotide sequence in a gene that does not code for the gene product. One component of an intron that often increases expression in monocots is the Adh1 intron. This component of the construct is optional.

[0149] The transit peptide-coding region is a nucleotide sequence that encodes for the translocation of the protein into organelles such as plastids and mitochondria. It is preferred to choose a transit peptide that is recognized and compatible with the host in which the transit peptide is employed. In this invention the plastid of choice is the amyloplast. An example is Ferredoxin transit peptide that worked well for us in the past.

[0150] It is preferred that the hybrid polypeptide be located within the amyloplast in cells such as plant cells that synthesize and store starch in amyloplasts. If the host is a bacterial or other cell that does not contain an amyloplast, there need not be a transit peptide-coding region.

[0151] A terminator is a DNA sequence that terminates the transcription. The fusion polypeptides may also include post-translational modifications known to the art such as glycosylaiton, acylation, and other modifications not interfering with the desired activity of the polypeptide.

[0152] Brief Description of the Procedure for Developing Fusion Polypeptide

[0153] A genetic construct encoding a fusion of the invention may be obtained by “combining” the nucleotide sequences encoding at least one desired protein or polypeptide with at least one nucleotide sequence that codes for “GLYTR” or “GLASS” domains optionally with or via one or more sequences that encode a “LINKR” and “CTEND” sequences as described above, in such a way that expression of the combined sequences in the desired plant or any other organism leads to the formation of the fusion.

[0154] Genes can be cut and changed by ligation, mutation agents, digestion, restriction and other such procedures for example, as outlined in Sambrook et al., “Molecular Cloning: A Laboratory Manuel”, 2^(nd) edition, Vols1-3, Cold Spring Harbor Laboratory(1989).

[0155] In addition, the sequences encoding for the “GLYTR” or “GLASS” domains ,“LINKR” and “CTEND” regions can be provided synthetically using known DNA synthesis techniques or isolated from a suitable biological source.

[0156] In addition to the elements mentioned above, the genetic construct encoding the fusion proteins of the invention may further contain all other elements known per se for nucleic acid sequences or genetic constructs, such as other control elements, terminators, translation or transcription enhancers, integration factors, signal sequences, and selection markers etc., that are preferably suited for use in the transformation of the host plant. The sequences that encode these further elements of the construct may be isolated from a biological source or synthesized synthetically. The one or more nucleotide sequences encoding these elements of the construct again can be combined with the nucleotide sequence encoding the fusion in a manner described in in Sambrook et al., “Molecular Cloning: A Laboratory Manuel”, 2^(nd) edition, Vols.1-3, Cold Spring Harbor Laboratory(1989). The genetic construct encoding the fusion proteins may also include post-translational modifications known to the art such as glycosylation, acylation, and other modifications not interfering with the desired activity of the polypeptide.

[0157] Construct Development

[0158] According to one preferred embodiment, the genetic construct encoding the fusion is preferably in a form suitable for transformation of a plant, such as a vector or plasmid. The recombinant nucleic acid sequence of this invention is inserted into a convenient cloning vector or plasmid. For the present invention the preferred host is a starch granule-producing organism. However, bacterial hosts can be employed. In bacterial host, transcriptional regulatory promoters include lac, TAC, trp and the like. Additionally, DNA coding for transit peptide most likely would not be used and a secretory leader that is upstream from the structural gene may be used to get the polypeptide into the medium. Alternatively, the product is retained in the host and the host is lysed and the product isolated and purified by starch extraction methods or by binding the material to a starch like matrix such as amylose, or amylopectin, glycogen or the like to extract the product.

[0159] The cloning vector may contain coding sequences for a transit peptide to direct the plasmid into the correct location. Examples of transit peptide sequences are shown in

[0160] Coding sequences for other transit peptides can be used. Transit peptides naturally occurring in the host to be used are preferred.

[0161] Attached to the transit peptide coding sequence is the DNA sequence encoding the N-terminal end of the fusion protein domain. The direction of the sequence encoding the fusion protein is varied depending on whether sense or antisense transcription is desired. DNA constructs of this invention specifically described herein have the sequence encoding the “GLASS” domain at the N-terminus end but the “GLYTR” domain can also be at the N-terminus end and the “GLASS” sequence following. The same procedure applies to inserting “LINKR” and “CTEND” regions if needed. At the end of theDNA construct is the terminator sequence. Such sequences are well known in the art.

[0162] The cloning vector is transformed into a host. Introduction of the cloning vector, preferably a plasmid, into the host can be done by a number of transformation techniques known to the art. These techniques may vary by host but they include microparticle bombardment, micro-injection, Agrobacterium transformation, electroporation, and the like. If the host is a plant, the cells can be regenerated to form plants. Methods of regeneration of plants is known in the art. Once the host is transformed and the proteins expressed therein, the presence of the DNA encoding the fusion protein in the host is confirmed. Transcript levels can be measured and the presence of fusion proteins may b econfirmed by Western blotting or ELISA or as a result of change in the Theological properties of starch.

[0163] With regard to starch synthase fusion proteins, WO 98/14601 provides similar methods to generate naturally occuring starch that has been modified to comprise the payload peptide and not associated with bringing any structural changes to the starch or glucan chain lengths. The present invention is based, in part, on the further discoveries regarding SS enzymes and their constituent domains (detailed information provided herein below) and further evidence for the mechanism of protein entrapment in the starch granules. The present invention provides therefore methods for making and using ‘starch synthase fusion proteins’ and producing transgenic plants capable of producing “structurally modified starch” or starch granules as described herein below. Such “structurally modified starch” of the present invention differs from naturally occurring starch in the plant by at least one property thereof, such as crystallinity, branching degree, glucan composition and glucan chain length.

[0164] With regard to sequences of the starch association domain, WO 98/14601 described the idea of a hybrid polypeptide comprising: (a) a starch binding domain, and (b) payload polypeptide fused to said starch binding domain. Said starch binding domain is referred as “starch-encapsulating domain”. It may be any starch binding domain known per se, for instance derived from soluble starch synthase I, IIa, IIb, Du1, GBSS, branching enzyme I, IIa, IIb, and/or glucoamylase polypeptides. The present invention provides, in at least one embodiment, a polypeptide sequence of GBSS that will enable fusion proteins to be entrapped in the granular matrix.

[0165] With regard to structural modification of starch, WO 98/14601 provides a “peptide-modified starch” for nutritious feed. WO 98/14601 provides for encapsulation of desired amino acids or peptides within starch and specifically within starch granule to increase the plants capacity to produce a specific protein, peptide or provide an improved aminoacid balance. WO 98/14601 defined modified starch as the naturally occurring starch that has been modified to contain a payload polypeptide. Payload polypeptides are described therein as hormones or other medicaments, e.g. insulin in a starch encapsulating form to resist degradation by stomach acids for producing the payload polypeptides in easily purified form or to enhance the amino acid content of particular amino acids in the starch to provide grain feeds enriched in certain amino acids. The present invention provides, in some embodiments, methods of making and using “structure-modified starch”, such as may be used in various industrial applications.

[0166] WO 98/14601, provides for a payload polypeptide which is not endogenous to the starch encapsulating region whose expression is desired in association with this region to express a starch containing the payload polypeptide. Specific examples of payload polypeptides described therein are hormones, eg. Insulin, a growth factor like somatotropin, calcitonin, beta endorphin, urogastrone, beta globin, myoglobin, human growth hormone, angiotensin, proline, proteases, beta-galoctosidase, and cellulase, antibody, an enzyme, immunoglobulin, or dye, prolactin, and serum albumins etc.

[0167] The present invention provides polypeptides, in at least one embodiment, which are capable of interacting with starch or starch granules and show an affinity and/or enzymatic activity with starch, such that the polypeptides of the present invention may be associated with modifying glucan chain lengths of amylopectin. The present invention further provides for fusion proteins containing one starch association domain and one catalytic domain of SS enzyme that alters, converts and modifies starch structure. The present invention provides a means and methods therefore to modifying starch structure.

[0168] II. Domains of the Enzymes Involved in Starch Metabolism and their Potential Uses

[0169] Enzymes, particularly from microorganisms, are known that interact with starch. These enzymes generally contain one or more catalytic domain, and one or more regions that can bind to starch or starch granules and referred to as “starch binding domains” or “starch binding regions”. Starch association-domains for starch synthesis enzymes in higher plants however are not known or described in the literature.

[0170] Svensson et al., Biochem. J. (1989), 264, 309-311, described the sequence homology between putative starch binding domains from α-amylase from Streptomyces limosus, β-amylase from Clostridium thermosulfurogenes, glucoamylase from A.niger, maltogenic α-amylase from Bacillus stearothermophilus, malto-tetraose forming amylase from Pseudomonas slutzeri, CGTase from Bacillus, CGTase from Klebsiella pneumoniae and glucoamylase from Rhizopus oryzae. Various starch-binding domains were also compared by Janecek& Sivcek, 1999 (FEBS letters 456, 119-125). It has been suggested that some conserved tryptophan residues and the amino acids directly adjacent may play an important role in starch binding (vide Goto et al., Appl. Environ.Microbiol.,1994, p3926-3930, Chen et al., Protein engineering, 1995, Vol 8:1049-1055, Williamson et al., Biochemistry, 1997, 36:7535-7539). Chen et al., 1991, Gene 99, 121-126, Biotechnol. Prog. 1991, 7: 225-229 described a fusion of B3-galactosidase and the starch-binding domain from an Aspergillus glucoamylase, plasmids encoding such a fusion, and expression in E. coli. The starch-binding region is used to increase the affinity of β-galactosidase for starch granules, in particular as an affinity tail for recovery or enzymatic immobilization using native starch granules as an absorbant.

[0171] The use of starch binding domain fusions in oral care compositions that contain such fusions is described in the patent WO 98/16190. The fusions were prepared by expression of an appropriate expression vector in a suitable microorganism. WO 99/15636 describes starch-binding domains, and in particular the “D” and “E-domains” of the maltogenic amylase from Bacillus StearothermophilusC599, and expression thereof in a Bacillus host cell. This patent also described fusions of starch binding domain and a reporter gene such as GFP to monitor the expression of the starch binding domains in the Bacillus host. This patent only describes expression in Bacillus host and does not describe fusion of starch binding domain and an enzyme that can interact with starch or starch granule.

[0172] Dalmia et al., Biotechnology and Bioengineering, 1995, 47:575-584 described fusions of β-galoctosidase and the starch binding domains of glucoamylase I of Aspergillus awamori and of cyclodextrin glucanotransferase (domain E of CGTase) from Bacillus macerans, respectively, plasmids encoding such fusions, and expression of said fusions in E. coli. The fusion proteins thus obtained are said to bind specifically to potato starch, corn-starch, and cross-linked amylose. As a possible application, the use of the starch binding domains as an “affinity tag” is suggested. Similarly, Dalmia et al., 1994, Enzyme Microb.Technol, vol 1. describe fusions containing a starch binding domain from Aspergillus niger glucoamylase, which is again used as an affinity tail to facilitate the one step purification of the target β-galactosidase. The use of cellulose binding domains as an affinity tag for protein purification (i.e. a fusion of a cellulose binding domain from cellulase and a-galactosidase) has also been described in the art by vide Ong et al., 1989, Trends in Biotechnology, 7:239-243.

[0173] All the above references describe fusions of a starch binding domain and an enzyme, said fusions are only expressed in micro-organisms such as E. coli. The starch binding domain is included only as a “tail” or tag in order to facilitate the isolation and purification of the desired enzyme activity from the bacterial culture medium.

[0174] The use of fusion proteins in plants in situ, in particular entrapped in the starch granules has not been previously described in the literature. WO 98/14601 describes entrappment of a “payload polypeptide” in order to make a nutritionally enriched starch. The expression in plants of fusions containing enzyme doamins that can alter the length of glucan chains in amylopectin, and there by produce modified starch had not been described or suggested however in the literature.

[0175] The present application provides a means of altering starch structure and deposition in plants by using novel starch synthesizing enzymes whose catalytic properties have been found to be substantially different from known enzymes. Starches produced in plants expressing these enzymes, which are also provided by the present invention, are substantially new and novel.

[0176] The genetic constructs described in this patent may be of plant, fungal, bacterial or animal origin, and are generally incorporated into the plant genome by sexual crossing or by transformation. The enzyme gene products may be an additional copy of a wild-type gene or may encode a modified enzyme with improved properties. Incorporation of the enzyme gene construct(s) into crop plants may have varying effects depending on the amount and type of enzyme gene(s) introduced. It may also increase the plant's capacity to produce starch, in particular by altering the temperature optimum for enzyme activity, giving increased yield. It may also result in production of starch with an altered fine structure (or quality) as the exact structure depends on the novel enzyme introduced. In examples where starch structure has been altered there have generally been starch-synthesizing enzymes expressed in a wild-type background via sexual crossing. The following patent applications describe this concept in detail: PCT/GB92/01881; US application numbers 4,35,020 and 9,30,935, European publication number EPA 3,68,506 (published May 16, 1990); UK patent application number 9,218,185.8. The disclosures of these applications are hereby incorporated by reference.

[0177] III. Starch Synthases

[0178] Both prokaryotic and eukaryotic cells use polysaccharides as a storage reserve. In the prokaryotic cell the primary reserve polysaccharide is glycogen. Although glycogen is similar to the starch found in most vascular plants it exhibits different chain lengths and degrees of polymerization. In many plants, starch is used as the primary reserve polysaccharide. Starch is stored in the various tissues of the starch bearing plant. Starch is made of two components in most instances; one is amylose and the other amylopectin. Amylose is formed as essentially linear glucans and amylopectin is formed as a more highly-branched chains of glucans. Typical starch has a ratio of 25% amylose to 75% amylopectin. Starch synthases (EC 2.4.1.11) elongate starch molecules and act on both amylose and amylopectin. Starch synthase (SS) activity can be found associated both with the granule and in the stroma of the plastid. Variations in the amylose to amylopectin ratio in a plant can affect the properties of the starch. Additionally starches from different plants often have different properties. Maize starch and potato starch appear to differ due to the presence or absence of phosphate groups. Certain plants' starch properties differ because of mutations that have been introduced into the plant genome. Mutant starches are well known in maize, rice, and peas and the like.

[0179] The changes in starch branching or in the ratios of the starch components result in different starch characteristic. One characteristic of starch is the formation of starch granules that are formed particularly in leaves, roots, tubers and seeds. These granules are formed during the starch synthesis process. Certain synthases of starch, particularly granule-bound starch synthase, soluble starch synthases and branching enzymes are proteins that are “granule bound” within the starch granule when it is formed (Smith et al., 1997, Ann. Rev. Plant Physiol.Plant Mol. Biol. 48, 67-87).

[0180] Different isoforms of soluble starch synthase have been identified and cloned in pea (Denyer and Smith, 1992, Planta 186: 609-617; Dry et al., 1992, Plant Journal, 2: 193-202), potato (Edwards et al., 1995, Plant Physiol 112: 89-97; Marshall et al., 1996, Plant Cell 8: 1121-1135), wheat (Gao and Chibbar, 2000; Genome. Vol 43: 768-775), and in rice (Baba et al., 1993, Plant Physiol. 103: 565-573), while barley appears to contain multiple isoforms, some of which are associated with starch branching enzyme (Tyynela and Schulman, 1994, Physiol. Plantarum 89: 835-841).

[0181] The capacity for starch association of the bound starch synthase enzyme is well known. Various enzymes involved in starch biosynthesis are now known to have differing propensities for binding as described by Mu-Forster et al. (1996, Plant Phys. 111: 821-829). Granule-bound starch synthase (GBSS) activity is strongly correlated with the product of the waxy gene (Shure et al., 1983, Cell 35: 225-233). The synthesis of amylose in a number of species such as maize, rice and potato has been shown to depend on the expression of this gene (Tsai, 1974, Biochem Gen 11: 83-96; Hovenkamp-Hermelink et al., 1987, Theor. Appl. Gen. 75: 217-221). Visser et al. described the molecular cloning and partial characterization of the gene for granule-bound starch synthase from potato (1989, Plant Sci. 64(2):185-192).

[0182] In starch producing plants starch is usually synthesized in the form of starch granules. A number of enzymes in the plant especially the ones involved in the starch synthesis and degradation interact in vivo with these granules. These include the enzymes such as starch synthases, branching enzymes and debranching enzymes, and amylases etc. for which reference is made to Mu, C., Ham, C., Ko, Y. T., Singletary, G. W., Keeling, P. L. and Wasserman, B. P. Plant J., 1994, 6:151-159, Smith, A. M., Denyer, K., and Martin, C. Annu.Rev.Plant Physiol. Mol. Biol., 1997, 48:67-87 and Martin C., and Smith A.M. The Plant Cell, 1995, 7:971-985. However, compared to any other enzyme, granule bound starch synthase (GBSS) is the most abundant protein entrapped in the starch granules with highest affinity to amylopectin.

[0183] The present invention also classifies maize α-1,4 glucan transfereases or starch synthases based on their specificities to process various lengths of α-1,4 glucan chains in the amylopectin cluster. For example, according to the present invention, SS enzymes are defined in 4 classes. ‘Class I’ enzymes that include maize SSI and like enzymes, and preferentially elongate α-1,4 glucan chains to synthesize shorter A and B1 chains; ‘Class II’ enzymes that include maize SSIIa and SSIIb and like enzymes, and preferentially add a glucose unit(s) to α-1,4 glucan chains to synthesize longer A and B1 chains and intermediate B2 or B3 chains; ‘Class III’ enzymes that include maize SSIII and preferentially add a glucose unit(s) to α-1,4 glucan chains to synthesize longer A, B1, B2 and B3 chains as well as longer B3 or C chains of amylopectin. “Class IV” enzymes include GBSS and preferentially add a glucose unit(s) to α-1,4 glucan chains to synthesize longer B3 or C chains of amylopectin as well as amylose. In maize or any other crop when transformed to express or overexpress any one specific class of starch synthases described above will result in an increased number of glucan chains in that specific class. This patent application relates to modification of starch structure by introduction/entrapment of polypeptide domains of other soluble starch synthases (SSS) in addition to GBSS (in the form of GBSS+SSS enzyme fusion proteins) within the starch granule matrix. Therefore, the present invention provides new starch synthases other than GBSS or SSI within the starch granule matrix. These enzymes contain starch association domain of either GBSS or SSI as described above and herein which provides starch association properties similar to wild type GBSS or SSI while retaining the α-1,4 glucan transferase activity (catalytic activity) of either GBSS or soluble starch synthases such as GBSS, SSI, SSIIa, SSIIb, and SSIII and the like. Starches produced in plants expressing these enzymes are substantially new and novel.

[0184] The use of cDNA clones of animal and bacterial glycogen synthases are described in PCT/GB92/01881. The use of cDNA clones of plant soluble starch synthases has been reported. For example, the amino acid sequences of pea soluble starch synthase isoforms I, and II were published byDry et al. (1992, Plant Journal, 2:193-202) and SSIII (Gao et al., 1998). The amino acid sequence for rice soluble starch synthase was described by Baba et al.,(1993, Plant Physiology). This last sequence (rice SS) incorrectly cites the N-terminal sequence and hence is misleading. Presumably this is because of some extraction error involving a protease-degradation or other inherent instability in the extracted enzyme. The correct N-terminal sequence (starting with AELSR) is present in what they refer to as the transit peptide sequence of the rice SS.

[0185] Branching enzyme [α1,4Dglucan: α 1,4Dglucan 6D(α1,4Dglucano) transferase (E.C. 2.4.1.18)], some times called Q-enzyme, converts amylose to amylopectin. A segment of a α 1,4Dglucan chain is transferred to a primary hydroxyl group in a similar glucan chain. Bacterial branching enzyme genes and plant sequences have been reported (rice endosperm: Nakamura et al., 1992, Physiologia Plantarum, 84:329-335 and Nakamura and Yamanouchi, 1992, Plant Physiol., 99:1265-1266; pea: Smith, 1988, Planta, 175:270-279 and Bhattacharyya et al., 1990, J. Cell Biochem., Suppl. 13D:331; maize endosperm: Singh and Preiss, 1985, Plant Physiology, 79:34-40; VosScherperkeuter et al., 1989, Plant Physiology, 90:75-84; potato: Kossmann et al., 1991, Mol. Gen. Genet., 230(12):39-44; cassaya: Salehuzzaman and Visser, 1992, Plant Mol Biol, 20:809-819). The sequence of maize branching enzyme I was investigated by Baba et al., 1991, BBRC, 181:87-94. Starch branching enzyme II from maize endosperm was investigated by Fisher et al.(1993, Plant Physiol., 102:1045-1046). The use of cDNA clones of plant, bacterial and animal branching enzymes have been reported. The nucleotide and amino acid sequences for bacterial branching enzymes (BE) are known from the literature. For example, Kiel et al. cloned the branching enzyme gene glgB from Cyanobacterium synechococcussp PCC7942 (1989, Gene (Amst), 78(1): 918) and glycogen branching enzyme gene (glgB) from Bacillus stearothermophilus and expressed in Escherichia coli and Bacillus subtilis Kiel J A. Boels J M. Beldman G. Venema G. (1991, Molecular & General Genetics. 230(1-2):136-44). The genes glc3 and gha1 of S. cerevisiae are allelic and encode the glycogen branching enzyme (Rowen et al., 1992, Mol. Cell Biol., 12(1): 22-29). Matsumomoto et al. investigated glycogen branching enzyme from Neurospora crassa (1990, J. Biochem., 107:118-122). The GenBank/EMBL database also contains sequences for the E. coli glgB gene encoding branching enzyme.

[0186] A common characteristic of SS clones is the presence of a KXGGLGDV consensus sequence that is believed to be the ADP-Glc binding site of the enzyme (Furukawa et al., 1990, J Biol Chem 265: 2086-2090; Furukawa et al., 1993, J. Biol. Chem. 268: 23837-23842). See below for example, the SS enzymes from various organisms

[0187] Granule Bound Starch Synthases (GBSS)

[0188] Accession Numbers:

[0189] gi|2833387|sp|Q43654|;gi|2833377|sp|;gi|2833381|sp|Q42857|; gi|2833388|sp|Q43784|gi|2829792|sp|P93568|; gi|2833383|sp|Q43092|; gi|136757|sp|P04713|; gi|136755|sp|P09842|; gi|267196|sp|Q00775|gi|2833382|sp|Q42968|; gi|2833384|sp|Q43093|; gi|6136121|sp|082627|; gi|2833385|sp|Q43134|;gi|136765|sp|P27736|; gi|2833390|sp|Q438471; gi|136758|sp|P19395|; gi|2833389|sp|Q43846|;gi|2842612|sp|Q59001|; gi|2811062|sp|O08328|; gi|729578|sp|P39125|; gi|2829618|sp|P74521|; gi|1169908|sp|P08323|; gi|121295|sp|P05416|; gi|729577|sp|P39670|; gi|1169909|sp|P45179|;

[0190] Soluble Starch Synthases (SSS)

[0191] Accession Numbers

[0192] gi|2129898|pir||S61505;gi|7489826|pir||T01265;gi|9502143|gb|AAF87999.1|AF258608_(—)1 gi|2833390|sp|Q43847|;gi|7489274|pir||T07663;gi|4582789|emb|CAB40374.1|;gi|8573760|g b|AAC17969.2|;gi|8953573|emb|CAB96627.1|;gi|2833384|sp|Q43093 |;gi|12019656|gb|AAD 45815.2|gi|2833387|sp|Q43654|;gi|6467503|gb|AAF13168.1|AF173900_(—)1;gi|7433871 |pir||S7 4473gi|7188796|gb|AAF37876.1|AF234163_(—)1;gi|8708896|gb|AAC17970.2|;gi|8953571 |emb |CAB96626.1|;gi|2833389|sp|Q43846|;gi|10177090|dbj|BAB10396.1|;gi|9502145|gb|AAF88 000.1|;gi|7489695|pir||T06798;gi|5825480|gb|AAD53263.1|AF155217;gi|9369336|emb|CAB 99210.1|gi|8901183|gb|AAC17971.2|;gi|5880466|gb|AAD54661.1|;gi|2829792|sp|P93568|; gi|7488349|pir||T04926;gi|3192881|gb|AAC19119.1|;gi|7529653|emb|CAB86618.1|;gi|6103 327|gb|AAF03557.1|;gi|7489712|pir||T01414;gi|7489711|pir||T01209;gi|9369334|emb|CAB9 9209.1|gi|5295947|dbj|BAA81848.1|; gi|549232|dbj|BAA07396.1|;gi|7489710|pir||T01208;gi|2833377|sp|Q40739|; gi|729578|sp|P39125|; gi|3688125|emb|CAA06959.1|;gi|9587348|gb|AAF89274.1|; gi|9587352|gb|AAF89276.1|AF286003_(—)1|;gi|9587319|gb|AAF89261.1|AF285986_(—)1|;gi|9587 329|gb|AAF89266.1|AF285991_(—)1;gi|9587337|gb|AAF89270.1|AF285995_(—)1;gi|9587313|gb|AAF89258.1|AF285983_(—)1|gi|9587317|gb|AAF89260.1|AF285985_(—)1;gi|9587311|gb|AAF892 57.1|AF285982_(—)1

[0193] gi|9587295|gb|AAF89249.1|AF285974_(—)1;gi|9587307|gb|AAF89255.1|AF285980_(—)1;gi|9587 321|gb|AAF89262.1|AF285987_(—)1;gi|9587297|gb|AAF89250.1|AF285975_(—)1;gi|958730|gb|AAF89252.1|AF285977;1,gi|9587339|gb|AAF89271.1|AF285996_(—)1;gi|958733|gb|AAF892 67.1|AF285992_(—)1

[0194] gi|9587305|gb|AAF89254.1|AF285979_(—)1; gi|9587335|gb|AAF89269.1|AF285994_(—)1; gi|958 7341|b|AAF89272.1|AF285997_(—)1; |gi|9587343|gb|AAF89273.1|AF285998_(—)1; gi|9587325|g b|AAF89264.1|AF285989_(—)1; gi|9587293|gb|AAF89248.1|AF285973_(—)1; gi|95873231 |gb|AAF 89263.1|AF285988_(—)1gi|9587333|gb|AAF89268.1|AF285993_(—)1; gi|9587299|gb|AAF89251.1|AF285976_(—)1; gi|9587327|gb|AAF89265.1AF285990_(—)1; gi|9587309|gb|AAF89256.1|AF28 5981_(—)1; gi|9587303|gb|AAF89253.1|AF285978_(—)1

[0195] Hybrid proteins or fusion proteins are polypeptide or peptide chains that contain two or more proteins or peptides fused together into a single polypeptide or peptide. Any of the starch synthase protein domains from the above listed or unlisted may be recombined as an embodiment of the present invention so as to control the interaction between SS and its substrates amylose or amylopectin. Such a recombination will allow to control the glucan chain lengths synthesized in the starch granule and therefore, control the useful properties of the starch.

[0196] IV. Glucan Association and Chain Length Specificity Characteristics of SS Enzymes:

[0197] Glucan-affinity gel electrophoresisin was used, and is described herein, as a tool to discover the precision and mechanism of interaction between the starch synthase enzymes, SSI, and GBSS, and their glucan-substrates, with which the glucan chain-lengths are determined by various starch synthases. SSI was found to have a greatly elevated affinity for increasing chain lengths of α-1,4 glucans (FIG. 8, A, B, C). Contrarily, the activity of SSI enzyme was decreased with increase in the avg. OCL of a-1, 4 glucans (FIG. 8D). Deletion of the N-terminal arm of SSI protein did not affect any of the glucan-binding characteristics (FIG. 9). Moreover, SSI enzyme activity is proportional to the average outer chain lengths of a given glucan molecule, which explains why SSI enzyme rate of catalysis is higher using glycogen (with shorter outer chains of dp ˜6.5) than with starch (avg. OCL ˜14.5) or amylopectin (avg. OCL˜11.5) (Imparl-Radosevich et al., 1998a; and references there in). During enzyme catalysis using SSI, majority of the 14C-label was incorporated into glucan chains with average dp less than 10 (FIGS. 10A & B). In contrast, GBSS displayed least affinity to glycogen (Table 1), however, with increasing outer chain lengths of glycogen, GBSS was found to have both an elevated affinity (FIG. 11) and catalytic activity (FIG. 11). The enzyme had the highest affinity for amylopectin and it preferred longer chains (>dp 20) of this molecule for chain extension as well (FIG. 11). In order to validate these results using SSI or GBSS, results to SSIIa, which does not entrap in the starch during the synthesis of starch granule, were compared. Unlike GBSS or SSI enzymes, SSIIa did not have any preference either for binding or for catalytic activity (FIGS. 12 and 13). SSIIa did not have any increased glucan binding with increase in the outer chain lengths. The activity of SSIa and Du 1 did not increase or decrease by altering the average outer chain lengths of glucan (FIG. 13). SSIIb did not prefer longer chained glycogen, but unlike SSI, the activity did not sharply drop after average outer chain length of dp 9. However, this drop occurred at average outer dp of 14 (FIG. 13). These contrasting results among the different enzymes that are exemplified herein indicate that the starch synthase enzymes ability to associate with the carbohydrate chains enable the enzyme to be entrapped inside the starch granule. Moreover, each enzyme has it's own specificity for length of the glucan chains. These findings provide a basis for explaining why GBSS and SSI are more strongly associated with the starch granules whereas SSIIa and SSIIb are poorly or not associated with the granule.

[0198] V. GLucan ASSociation Domain (GLASS Domain) of GBSS

[0199] Using GBSS enzyme, it has been demonstrated that the glucan-binding domain is not discrete at N- or C-terminus, but may be located close to the amino acid number 103 of the protein. The smallest peptide that has affinity for glucan was found to be about 18 kDa. The C-terminal region of GBSS (˜20 amino acids long) proteins from a wide range of species is conserved, and is hydrophilic and carries a net negative charge. This C-terminal extension is absent from other starch synthase isoforms and bacterial glycogen synthases. Edwards et al. (1999) have shown that this C-terminal region of the enzyme in potato confers most of the specific properties of this isoform except its processive elongation of glucan chains. This C-terminus of maize GBSS has been shown herein not be involved in binding of the enzyme to amylopectin molecule. Sequence comparison of starch synthases from different plant species reveal that in the region of the protein following the amino acid residue number 103 is highly conserved especially for GBSS enzymes as compared to soluble starch synthases. Within this 18 kDa starch associating domain, amino acid sequence “PV(L)AGT” starting at residue number 107 is highly conserved among pea, potato and in maize GBSS. There is also another sequence starting at residue number 155, “NDWHT” which is highly conserved among all known SS enzymes in maize. Therefore, one or more of these conserved regions may confer glucan-binding properties to GBSS enzyme. Overall, it is clear that the starch-affinity domain of SS enzymes is structurally different from the starch-binding domain of the degradative enzymes and unlike these enzymes, is not a single discrete domain.

[0200] The present invention provides a glucan or starch association domain of a starch synthase, such as a granule bound starch synthase peptide or soluble starch synthase which is, in one embodiment, about 18 kDa molecular weight under reducing conditions. The starch association domain of the present invention is preferably a peptide or polypeptide fragment of granule bound starch synthase (GBSS), which has an N-terminal end which is within, at most, 50 amino acids of the amino acid corresponding to about amino acid 103 of maize GBSS enzyme. Preferably, the starch association domain of the present invention has an N-terminal end which is within, at most, 50 amino acids of the amino acid corresponding to amino acid 103 of maize GBSS and extends, at most, approximately a further 200 amino acids along toward the C-terminus of GBSS enzyme. Alternatively, the association domain of the present invention has an N-terminus as described above and a C-terminus which is within, at most, 52 amino acids of the amino acid corresponding to amino acid 148 of maize GBSS. Alternatively, the association domain of the present invention is a peptide or polypeptide of GBSS corresponding to an amino acid sequence spanning amino acid positions 103±50 amino acids to about amino acid position 251±50 amino acids of the maize GBSS enzyme. Alternatively the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 40 amino acids from the amino acids corresponding to the amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 30 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 20 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 10 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 5 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 4 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to an amino acid position which are, independently, plus or minus 3 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectfully, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 2 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 1 amino acids from the amino acids corresponding to amino acid positions 103 and 251, respectively, of maize GBSS enzyme.

[0201] VI. Determination of the GLYcosyl TRansferase Domain (GLYTR Domain) of SS Enzymes

[0202] Using glucan affinity gel electrophoresis, and using SSI enzyme, the other smallest peptide that has affinity for glucan was found to be about 21 kDa. Within this 21 kDa starch associating domain, and with amino acid sequence starting the residue number 387 and with the following sequence LGLPIRPDVPLIGFIGRLD is highly conserved among all the starch synthases, and especially SSI, SSIIa, SSIIb and GBSS enzymes in maize. And, this region within or very close to the glycosyl transferase group I domain. Hence, it is highly likely that this region is involved in interaction with the glucan during the process of starch synthesis and glucan chain elongation. This is likely to be true for other SS enzymes as well due to their high sequence homology in this region. This observation also indicates that the glucosyl transferase function of SS enzymes invoves association or binding with the glucan polymer.

[0203] Therefore, the present invention provides a glycosyl transferase domain (Domain B) of a starch synthase that has affinity to glucan polymer, such as a soluble starch synthase I domain that is, in one embodiment, about 21 kDa molecular weight under reducing conditions. The glycosyl transferase domain (Domain B) of the present invention is preferably a peptide or polypeptide fragment of any starch synthase (SS), which has an N-terminal end which is within, at most, 50 amino acids of the amino acid corresponding to about amino acid 380 of maize SSI, SSIIa, SSIIb and GBSS enzymes and amino acid 1470 of maize SSIII or Du1 enzyme. Preferably, the glycosyl transferase domain of the present invention has an N-terminal end which is within 380 amino acids of maize SSI, SSIIa, SSIIb and GBSS enzymes and 1470 aminoacids of maize SSIII or Du1 enzyme, at most, 50 amino acids of the and extends, at most, approximately a further 200 amino acids along toward the C-terminus of each one of these enzymes. Alternatively, the association domain (Domain B) of the present invention has an N-terminus as described above and a C-terminus which is within, at most, 52 amino acids of the amino acid corresponding to amino acid 380 of maize SSI, SSIIa, SSIIb, and GBSS and amino acid 1470 of maize SSIII or Du1 enzyme. Alternatively, the glycosyl transferse domain (Domain B) of the present invention is a peptide or polypeptide of either SSI, SSIIa, SSIIb or GBSS corresponding to an amino acid sequence spanning amino acid positions 380±50 amino acids to about amino acid position 580±50 amino acids of the maize SS enzymes. Alternatively the N- and C-termini of the Glycosyl transferase domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 40 amino acids from the amino acids corresponding to the amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb, and GBSS enzyme; alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 30 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 20 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 10 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 5 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 4 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to an amino acid position which are, independently, plus or minus 3 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1);alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 2 amino acids from the amino acids corresponding to amino acid positions 380 and 580, respectively, of maize SSI, SSIIa, SSIIb and/or GBSS enzyme; and amino acid position 1470 and 1670, respectively of maize SSIII (Du-1); alternatively, the N- and C-termini of the association domain of the present invention may correspond to amino acid positions corresponding to amino acid positions which are, independently, plus or minus 1 amino acids from the amino acids corresponding to amino acid positions 378 and 545 for GBSS, 441 and 570 for SSI, 540-687 for SSIIa, 506 to 646 for SSIIb, and 1478 to 1600 for Du1 respectively.

[0204] The present invention preferably provides an isolated and/or purified domains, as described herein.

[0205] The above said “GLASS” and “GLYTR” domains of the present invention are alternatively defined as peptide or polypeptide amino acid sequences which are at least 80% identical or homologous with the above-described “GLASS” and “GLYTR”domains. Alternatively, the association domain of the present invention is more than 85% identical or homologous, or more than 90% identical or homologous or more than 95% identical or homologous, or more than 98% identical or homologous, or more than 99% identical or homologous, as compared with the above-described “GLASS” and “GLYTR”domains. One of ordinary skill in the art will readily be able to determine identical or homologous sequences by, for example, aligning sequences in question with the above-described sequence and calculating the percentage of amino acids which are different over the length of the above-described association domain. The identical or homologous peptide or polypeptide amino acid sequences of the present invention may also be identified, for example, by BLAST or Gapped BLAST search and/or comparisons, such as a comparison described or obtained by software obtainable from the NCBI website, such as through http://www.nih.gov, or http://www.ncbi.nlm.gov:80/BLAST/, or related site, or as described by Altschul, Stephen F. et al, 1997 “Gapped BLAST and PSI-BLAST: A new generation of protein data base search programs” Nucleic Acids Res. 25:3389-3402.

[0206] The above said “GLASS” and “GLYTR”domains of the present invention may also include conservative amino acid substitutions of the above-described association domain peptide or polypeptide. Such conservative amino acid substitutions will be recognized by one of ordinary skill in the art to include any of the following: Amino acids Synonymous groups Ser (S) Ser, Thr, Gly, Asn Arg (R) Arg, His, Lys, Glu, Gln Leu (L) Leu, Ile, Met, Phe, Val, Tyr Pro (P) Pro, Ala, Thr, Gly Thr (T) Thr, Pro, Ser, Ala, Gly; His, Gln Ala (A) Ala, Pro, Gly, Thr Val (V) Val, Met, Ile, Tyr, Phe, Leu, Val Gly (G) Gly, Ala, Thr, Pro, Ser Ile (I) Ile, Met, Leu, Phe, Val, Ile, Tyr Phe (F) Phe, Met, Tyr, Ile, Leu, Trp, Val Tyr (Y) Tyr, Phe, Trp, Met, Ile, Val, Leu Cys (C) Cys, Ser, Thr, Met His (H) His, Gln, Arg, Lys, Glu, Thr Gln (Q) Gln, Glu, His, Lys, Asn, Thr, Arg Asn (N) Asn, Asp, Ser, Gln Lys (K) Lys, Arg, Glu, Gln, His Asp (D) Asp, Asn, Glu, Gln Glu (E) Glu, Gln, Asp, Lys, Asn, His, Arg Met (M) Met, Ile, Leu, Phe, Val

[0207] Alternatively, such conservative amino acid substitutions may be any of those shown in the following: Amino acids Ser (S) Ser, Thr, Gln, Asn Arg (R) Arg, His, Lys Leu (L) Leu, Ile, Met, Phe, Val, Tyr, Ala, Trp Pro (P) Pro, Ala, Thr, Gly Thr (T) Thr, Ser, Ala, Trp, Gln Ala (A) Ala, Met, Ile, Leu, Phe, Val, Tyr, Trp Val (V) Val, Met, Ile, Tyr, Phe, Leu, Val, Ala Gly (G) Gly, Ala, Thr, Pro, Ser Ile (I) Ile, Met, Leu, Phe, Val, Ala, Tyr, Trp Phe (F) Phe, Met, Tyr, Ile, Leu, Trp, Val, Ala Tyr (Y) Tyr, Phe, Trp, Met, Ile, Val, Leu, Ala Cys (C) Cys, Ser, Thr, Met His (H) His, Arg, Lys Gln (Q) Gln, Gln, Asn, Thr, Ser Asn (N) Asn, Ser, Gln, Thr Lys (K) Lys, Arg, His Asp (D) Asp, Glu Glu (E) Glu, Asp Met (M) Met, Ile, Leu, Phe, Val, Ala, Tyr, Trp Trp (W) Trp, Met, Ile, Leu, Phe, Val, Ala, Tyr

[0208] The above said “GLASS” and “GLYTR”domain polypeptide or peptide of the present invention may be a soluble starch synthase, or granule bound starch synthase, branching enzyme, and any debranching enzyme from any cereal, such as maize, wheat, rice, sorghum or barley; a fruit-producing species such as banana, apple, tomato or pear; a root crop such as cassaya, potato, yam or turnip; an oil seed crop such as rapeseed, sunflower, oil palm, coconut, linseed or groundnut; a meal crop, such as soya, bean or pea; or any other suitable species.

[0209] The above said “GLASS” domain peptide or polypeptides of the present invention include a soluble starch synthase or GBSS of any of the above cereal, fruit-producing species, root crop, oil seed crop or meal crop, for example, or fragment thereof which preferably has an N-terminus corresponding to about amino acid 103± at most 50 amino acids of maize GBSS enzyme; more preferably corresponding to amino acid 103± at most 50 amino acids of maize GBSS enzyme, and extending, at most, approximately a further 200 amino acids along toward the C-terminus of the GBSS enzyme. In this embodiment, the glucan association domain peptide or polypeptide of the present invention may extend between any amino acid position corresponding to amino acids in the range of 53-153 of maize GBSS to any amino acid position corresponding to amino acids in the range of 98-198 of maize GBSS.

[0210] The above said “GLYTR” domain peptide or polypeptides of the present invention include a soluble starch synthase or GBSS of any of the above cereal, fruit-producing species, root crop, oil seed crop or meal crop, for example, or fragment thereof which preferably has an N-terminus corresponding to about amino acid 378±at most 50 amino acids of maize GBSS enzyme; 441±at most 50 amino acids of maize SSI enzyme; 540±at most 50 amino acids of maize SSIIa enzyme; 506+at most 50 amino acids of maize SSIIb enzyme; and 1478±at most 50 amino acids of maize Du1 enzyme and extending, at most, approximately a further 200±at most 50 amino acids along toward the C-terminus of the GBSS enzyme. In this embodiment, the glucan association domain or Domain “GLASS” peptide or polypeptide of the present invention may extend between any amino acid position corresponding to amino acids in the range of 53-153 of maize GBSS to any amino acid position corresponding to amino acids in the range of 98-198 of maize GBSS.

[0211] The present invention further provides a polypeptide or peptide as described above which is more than 85% identical or homologous, or more than 90% identical or homologous or more than 95% identical or homologous, or more than 98% identical or homologous, or 99% identical or homologous, as compared with the above-described association domain peptides or polypeptides, as described above.

[0212] The present invention further provides a glucan association domain peptide or polypeptide containing the following amino acid sequence:

[0213] SEQ. ID. No. 1 “KIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPYGEDV VFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPY YAEE”

[0214] The present invention also provides starch association domain peptides and polypeptides which are more than 85% identical or homologous, or more than 90% identical or homologous or more than 95% identical or homologous, or more than 98% identical or homologous, or more than 99% identical or homologous, as compared with SEQ ID No. 1 Such sequences of the present invention may be obtained or derived, for example, from any of the noted crops or plants, or from any of the sequences of the NCBI or other similar database, such as for example any of gi 136757, 2833385, 136755, 136758, 2833382, 136765, 2833388, 267196, 6136121, 2833381, 2833383, 2833377, 2833387, 2829792, 2833390, 2833384, 729578, 2811062, 1169908, 1169909, 2829618, 729577, 2833389, 1174879, 140977 or 549804 or any present in SEQ ID No. 1 wherein a sequence similar or identical or homologous to any one of SEQ ID No. 1, within the embodiments of the presently described invention may be found.

[0215] The present invention further provides starch synthase enzymes, such as starch synthase I (SSI), starch synthase II (SSIIa or SSIIb) or starch synthase III (SSIII) wherein the region in the SSI, SSIIa, SSIIb or SSIII, corresponding to amino acids 103±at most 50 amino acids, to about amino acid 148±at most 50 amino acids of GBSS has been altered, modified or made to be more homologous or identical to the sequence spanning amino acids 103±at most 50 amino acids to about amino acid 148±at most 50 amino acids of GBSS. One of ordinary skill will appreciate that the homology or identity in his region between SSI, SSIIa, SSIIb or SSIII to GBSS is about 70-80% on average. By altering or modifying or engineering SSI, SSIIa, SSIIb or SSIII enzymes, for example, according to the present invention, to contain a starch association domain more similar to GBSS, starch synthases are provided which contain the advantageous glucan association properties of GBSS while retaining, at least substantially, the catalytic properties of the starch synthases, such as SSI, SSIIa, SSIIb or SSIII. These altered or modified or engineered peptides or polypeptides will be capable of producing or containing, for example, a greater percentage of continuous glucan sequences in an amylopectin cluster than produced by wild-type starch synthases, thus providing changes in the confirmational structure of the amylopectin clusters.

[0216] The present invention therefore provides starch synthase enzymes, other than GBSS, which contain a starch association domain as described above and herein which provides starch association properties similar to wild-type GBSS while preferably retaining the α-1,4 glucan transferase (i.e., catalytic properties) of soluble starch synthases, such as SSI, SSIIa, SSIIb and SSIII.

[0217] In a further embodiment, the present invention provides soluble starch synthase enzymes, such as SSI, SSIIa, SSIIb or SSIII, containing glucan association domain polypeptides or peptides which are more than 80% to 90% identical or homologous to the GBSS glucan association domain peptide or polypeptide, or homologous or identical, as defined above and herein, in the region of the starch synthase enzyme corresponding to the GBSS glucan association domain defined above and herein.

[0218] Such further glucan association domain peptides and polypeptides may be compared with GBSS starch association domains of the invention by means known in the art and described herein. Such soluble synthase glucan association domains include, for example, the sequences of gi 2833377, gi 2833387, gi 2829792, and gi 2833389 or those shown above, which were obtained from a BLAST search. Similar, homologous or identical polypeptide or peptide amino acid sequences are provided by the present invention.

[0219] In a manner similar to that described above wherein soluble starch synthase enzymes are provided which contain a glucan association domain similar to or the same as GBSS, the present invention also provides granule bound starch synthases which contain a soluble starch synthase or soluble starch synthase-like glucan association domain, which is preferably more than 80% to 90% identical or homologous to a soluble starch synthase glucan association domain. Such an altered or modified granule bound starch synthase will preferentially provide continuous glucan sequences in an amylopectin cluster, for example, which are, on average, shorter than provided with wild-type GBSS. The modified, altered or engineered GBSS of this embodiment of the present invention provides changes in confirmational structure of amylopectin structures and, likely, amylose structure.

[0220] The modified, altered or engineered granule bound starch synthases or soluble starch synthases may include glucan association domains of different species. That is, for example, the present invention provides maize granule bound starch synthases or maize soluble starch synthases which may contain a starch association domain region or sequence which is obtained or derived from, or at least 85% (or at least 90%, or at least 95%, or at least 98%, or at least 99%) homologous or identical to a starch association domain of Basella alba, for example. In this manner, the present invention provides granule bound starch synthases and soluble starch synthases wherein the starch association domain is obtained from, derived from or at least 85% (or at least 90%, or at least 95%, or at least 98%, or at least 99%) homologous or identical to starch association domain of any cereal, such as maize, wheat, rice, sorghum or barley; a fruit-producing species, such as banana, apple, tomato or pear; a root crop such as cassaya, potato, yam or turnip; an oilseed crop such as rapeseed, sunflower, oil palm, coconut, linseed or ground nut; a meal crop, such as soya, bean or pea; or any other suitable species.

[0221] The present invention also provides starch synthases, such as soluble starch synthases and granule bound starch synthases of Basella alba (Malabar spinach) that are found to have higher affinity to glucan substrates. Moreover, the present invention provides starch synthases, such as soluble starch synthases or granule bound starch synthases of species other than Basella alba, such as those described above, which have been engineered, modified or altered to contain at least one of the catalytic peptide or polypeptide sequence or the starch association domain peptide or polypeptide sequence of Basella alba or fragments, or homologous sequence, thereof, as described above.

EXAMPLE I Expression of Fusion Proteins (Green Flourescent Protein (GFP), Metallothionein, and Citrate Synthase) Fused to Different GBSS Domains to Demonstrate that an Amino Acid Sequence of the Present Invention is Needed for Glucan Association of Expressed Recombinant Fusion Proteins

[0222] Affinity gel electrophoresis was used to demonstrate which one of the peptide domains of GBSS would associate with the glucan present in the native gels. For details on the Native gel electrophoresis, see below and the references listed herein as well as general knowledge in the art. The results of these experiments were compared with the genetic experiments by construction of plasmids carrying fusion proteins with different lengths of GBSS protein. Maize plants were transformed with the above said constructs. Transgenic plants containing the fusion protein were tested for both the levels of expression, and mainly the glucan (starch) association of the fusion protein. It was stunning that the peptide discovered from the biochemical experiments that had the glucan association properties was found to be the same that is required for glucan association of fusion proteins in transgenic maize plants.

[0223] The following constructs were made using fusion proteins of different lengths of GBSS protein and Green fluorescent protein (GFP), synthetic metallothinein and synthetic Pig heart citrate synthase. For the procedure on making constructs see below and herein as well as general knowldge in the art.

TABLE VI Summary of the analysis of the Fusion Proteins made with different domains of GBSS enzyme in maize kernels Plasmid Expressed Is the enzyme Entrapped in Identification Gene Construct in soluble Fraction? Active? the granules? I. pEXS 206 Transit peptide + GFP Yes NA No pEXS 208 Transit peptide + GFP + (N−) truncated (−97bp) GBSS Yes NA Yes pEXS 210 Transit peptide + GFP + full length GBSS Yes NA Yes pEXS 216 Transit peptide + (N−)truncated (−702bp)GBSS + GFP Yes NA No pEXS 218 Transit peptide + full length GBSS + GFP Yes NA Yes II. pEXS 224 Transit peptide + (N−)truncated (−300aa)GBSS + 1 × Metallothionein N.D NA No pEXS 228 Transit peptide + (N−)truncated (−300aa)GBSS + 10 × Metallothionein N.D NA No III. pEXS 233 Transit peptide + (N−)truncated (−482aa)GBSS + Citrate synthase Yes YES No pEXS 234 Transit peptide + (N−)truncated (−445aa)GBSS + Citrate synthase) Yes YES No pEXS 235 Transit peptide + (N−)truncated (−395aa)GBSS + Citrate synthase Yes YES No

[0224] TABLE VI A. Summary of Protein SEQ ID Nos: ENZYME and Protein Seq. Transit ID.No. peptide GLASS LINKR GLYTR CTEND GBSS-34 35-74  75-120 121-171 172-222 223-266 SS1-267 268-283 284-335 336-386 387-437 438-461 SSIIa-462 463-474 475-526 527-577 578-628 629-676 SSIIb-677 678-681 682-732 733-783 784-834 835-882 Du-I 883 884-932 933-982  983-1033 1034- 1085- 1084 1135 Seq.ID. Seq.ID. Seq.ID. “GLASS” No.s “GLYTR” No.s “CTEND” No.s GBSS: 1 GBSS: 1136 GBSS: 1146 SSI: 2 SSl: 1137 SSI: 1147 SSIIa: 3 SSIIa: 1138 SSIIa: 1148 SSIIb: 4 SSIIb: 1139 SSIIb: 1149 SSIII (Dul): 5 SSIII (Du1): 1140 SSIII (Dul): 1150

[0225] TABLE VI b Summary of Nucleotide Seq. ID. NO. s. Nucleotide sequence ID. No. s. GBSS: 1141 SSI: 1142 SSIIa: 1143 SSIIb: 1144 SSIII (Dul): 1145

[0226] TABLE VII A Cartoon showing GBSS domain required for starch granular entrapment (based on the transgenic analysis of various constructs for entrapment of recombinant proteins)

EXAMPLES:

[0227] TABLE VIII A Cartoon Showing the results from Biochemical evidence for the GBSS peptide required for its association to a glucan substrate in the gel.

[0228] EXAMPLE I (See FIGS. 14 and 15) demonstrates the following:

[0229] 1. Both biochemical and transgenic approaches identified the same peptide domain of GBSS as the Glucan Association Domain (Herein referred to as “GLASS” domain).Without presence of this particular domain, transgenic proteins did not associate with starch present in the endosperm of maize kernels. The “GLASS” domain is separate from glycosyl transferase domain (herein referred to as “GLYTR” domain in this patent). The order in which the proteins domains were fused did not matter for protein expression or glucan association as long as the “GLASS” domain was enclosed in the fusion protein. The present invention demonstrates that fusion protein technology of starch synthase enzymes may be applied in crop plants. Active fusion proteins were recovered with significant enzyme activity. The examples provided here demonstrate that the invention may be exemplified, without limitation, in maize crop.

EXAMPLE II. Examples of Some Possible and Functional Fusion Proteins

[0230] The “GLASS” and GLYTR” domains of various SS and GBSS enzymes were fused and the 3D-models for the recombinant fusion proteins are provided. Using Protein threading onto 3D-PSSM, all the starch synthase enzymes from maize were very well comparable with highest confidence to bacterial UTDP-N-acetylglucosamine 2-epimerase. Campbell et al.2000,Biochemistry 39:14993-15001, determined the X-ray structure of UDP-N-acetylglucosamine 2-epimerase with bound UDP and identified a high degree of structural homology to glycogen phosphorylase, and T4-phage β-glycosyl transferases. The relatioship of epimerase to these glycosyl transferses is very intriguing and a similarity to starch synthases is proposed herein as the starch synthase enzymes have the same glycosyl transferase function. It is also very intriguing that, Pfam00534 (glycosyl transferse family, group 1) domain is universal across all the starch synthases tested. FIGS. 16 and 17 show structures of UDP-N-acetylglucosamine 2-epimerase and glycogen phosphorylase created using the same database (Kelley et al., 2000, J. of Mol. Biol.299: 499-520.

[0231] EXAMPLE II (See FIGS. 16 and 17) demonstrates the following:

[0232] Fusion proteins from examples provided above displayed 3D folding very similar to the native proteins in vivo. This was accomplished when proper peptide lengths of fusions were made from “GLASS” and “GLYTR” domains. The 3D-structure of starch synthases is more closely related to UDP-N-Acetylglucosamine 2-epimerase and T4 phageB-glucosyltransferase than to glycogen phosphorylase. Also, for any fusion protein, the presence of highly conserved “Pfam 00534” domain results in similar protein folding at 3D level. Glucan transfer takes place in the catalytic or “GLYTR” domain of the present invention. One of the functions of “GLASS” domain is glucan binding as in GBSS, but also the chain length specificity is within this domain as well.

EXAMPLE III

[0233] Glucan Binding Properties of Starch Synthase Enzymes

[0234] Glucan affinity properties of various starch synthases (SS) enzymes from different plant species like banana fruit, basella leaf and carrot root, green bean pods, rice endosperm, rutabaga root, swetpotato root and wheat endosperm were examined and compared to maize endosperm SS forms. SSI enzyme from Basella alba displayed superior affinity to a given glucan (see table below) as compared to any of the maize enzymes studied so far. Therefore, the recombinant genes of SS enzymes from Basella and maize will enhance glucan-association properties of maize enzymes and thereby will result in better starch especially under adverse conditions. This transformation also results in altered amylopectin structure. TABLE IX A Comparison of K-values of Basella (B. alba L.) Starch Synthase like Enzymes with Maize SSI enzyme Substrate Enzyme Temperature (4° C.) Amylose Basella-Band 1 0.035^(a) Basella-Band 2 0.284 Maize SSI-2 0.35 Amylopectin Basella-Band 1 0.002 Basella-Band 2 0.004 Maize SSI-2 0.06 Glycogen Basella-Band 1 0.0186 Basella-Band 2 0.112 Maize SSI-2 1.20 Starch Basella-Band 1 0.006 Basella-Band 2 0.036 Maize SSI-2 0.09

[0235] A screen for starch synthase enzymes from different plant species and their affinities to glucan substrates was conducted. FIG. 18. shows SDS-electrophoresis and coomassie staining of proteins from various plants, namely banana fruit, basella leaf, carrot root, maize endosperm, green bean pods, rice endosperm, rutabaga root, sweetpotato root, and wheat endosperm. The proteins were run on native gel containing 2% boiled starch. The peptides or proteins that were bound to the glucan in the well were visualized by coomassie staining. And, were excised out of the native gel, and run on 10% SDS-gel. Very few peptides got bound to the glucan (data not shown). The proteins that were bound were transferred onto a nitrocellulose membrane for performing western blotting using maize SSI antibody. There was one protein in banana, two in basella, one in carrot, two or more in maize, one or two in green beans, two in ricen none in rutabaga and two in sweet potato, and two or three in wheat, were recognized by maize SSI antibody (Figure B). In order to confirm that these proteins that were bound to the glucan in the native gel and cross reacted with maize SSI antibody posses starch synthase activity, a renaturing gel was performed (see experimental procedures for details). These gels revealed both synthetic and degradative enzyme activity (Figure C) There were two proteins in banana, two in basella, one on corn, and two in wheat that possessed synthetic activity. Degradative enzyme activity was revealed in caroot, greenbean, sweetpotato and wheat (C). Figure D shows mobility of starch synthase enzymes of Basella alba in native gels containing no substrates (Controls). Also, starch synthase enzymes within maize endosperm have different affinities to glucans (See FIG. 19).

[0236] EXAMPLE III (See FIG. 19) demonstrates the following:

[0237] Various starch synthase enzymes have different affinities to a given glucan (FIG. 19). And, hence, it is possible to manipulate the functionality of native starch synthases and provide modifications to glucan chain lengths and starch structure.

[0238] The entire contents of the following references, along with the content of any references or documents or sequence deposit or other literature referred to and/or described herein or above or with the following are incorporated herein by reference in their entirety.

[0239] WO9720936 Starch Synthase Sequences

[0240] WO9844780 Starch Synthase Hosts

[0241] WO9814601 EnCapsulation

[0242] WO9924575 Dull1 Starch Synthase III

[0243] WO92/11376; 92/14827; 98/16190; 99/15636

[0244] PCT/GB92/01881

[0245] EPA 368506

[0246] U.S. Pat. Nos.: 5,792,920; 5,824,790; 5,859,333; 6,013,861; 6,107,060; 2,061,143; 4,789,557; 4,790,997; 4,774,328; 4,770,710; 4,798,735; 4,767,849; 4,801,470; 4,789,738; 9,30935;4,35,020; 4,792,458; 5,009,911; 5,300,145; 5,202,247; 5,137,819; 5,635,599; and 5,648,244.

[0247] UK Patent: 921818

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[0371] Vos-Scheperkeuter.-G. H.; Boer,-W.-de; Visser,-R. G. F.; Feenstra,-W. J.; Witholt,-B. (1986) Identification of granule-bound starch synthase in potato tubers. Plant-Physiol. 82 (2), 411-416.

[0372] Vos-Scheperkeuter,-G. H.; Wit,-J. G.-de; Ponstein,-A. S.; Feenstra,-W. J.; Witholt,-B. (1989) Immunological comparison of the starch branching enzymes from potato tubers and maize kernels. Plant-Physiol. 90 (1), 75-84. SEQ. ID. No. 1 Glucan Association Domain (“GLASS) of GBSS  “K I Y G P V A G T D Y R D N Q L R F S L L C Q A A L E A P R I L S L N N N P Y F S G P Y G E D V V F V C N D W H T G P L S C Y L K S N Y Q S H G I Y R D A K T A F C I H N I S Y Q G R F A F S D Y P E L N L P E R F K S S F D F I D G Y E K P V E G R K I N W M K A G I L E A D R V L T V S P Y Y A E E“ Seq ID. No. 2 Glucan Association domain (“GLASS”)domain (”GLASS”) of maize SSI E G I A E G S I D N T V V V A S E Q D S E I V V G K E Q A R A K V T Q S I V F V T G E A S P Y A K S G G L G D V C G S L P V A L A A R G H R V M V V M P R Y L N G T S D K N Y A N A F Y T E K H I R I P C F G G E H E V T F F H E Y R D S V D W V F V D H P S Y H R P G N L Y G D K F G A F G D N Q F R Y T L L C Y A A C E A P L I L E L G G Y I Y G Q N C M F V V N D W H A S L V P V L L A A K Y R P Y G V Y K D S R S I L V I H N L A H Q G V E P A S T Y P D L G L P P E W Y G Seq ID. No. 3 Glucan Association domain (“GLASS”)domain (“GLASS”) of maize SSIIa S K R R D P L Q P V G R Y G S A T G N T A R T G A A S C Q N A A L A D V E I K S I V A A P P T S I V K F P A P G Y R M I L P S G D I A P E T V L P A P K P L H E S P A V D G D S N G I A P P T V E P L V Q E A T W D F K K Y I G F D E P D E A K D D S R V G A D D A G S F E H Y G D N D S G P L A G E N V M N V I V V A A E C S P W C K T G G L G D V V G A L P K A L A R R G H R V M V V V P R Y G D Y V E A F D M G I R K Y Y K A A G Q D L E V N Y F H A F I D G V D F V F I D A P L F R H R Q D D I Y G G S R Q E I M K R M I L F C K V A V E V P W H V P C G G V C Y G D G N L V F I A N D W H T A L L P V Y L K A Y Y R D H G L M Q Y T R S V L V I H N I A H Q G R G P V D E F P Y M D L P E H Y L Q H F E L Y D P Seq ID. No.4 GlucanAssociation domain (“GLASS”)domain (“GLASS”) of maize SSIIb A D A A P A T D A A A S A P Y D R E D N E P G P L A G P N V M N V V V V A S E C A P F C K T G G L G D V V G A L P K A L A R R G H R V M V V I P R Y G E Y A E A R D L G V R R R Y K V A G Q D S E V T Y F H S Y I D G V D F V F V E A P P F R H R H N N I Y G G E R L D I L K R M I L F C K A A V E V P W Y A P C G G T V Y G D G N L V F I A N D W H T A L L P V Y L K A Y Y R D N G L M Q Y A R S V L V I H N I A H Q G R G P V D D F V N F D L P E H Y I D H F K L Y D N I G Seq ID. No. 5 GlucanAssociation domain (“GLASS”) of maize Du1 G G I Y D N R N G L D Y H I P V F G S I A K E P P M H I V H I A V E M A P I A K V G G L G D V V T S L S R A V Q D L G H N V E V I L P K Y G C L N L S N V K N L Q I H Q S F S W G G S E I N V W R G L V E G L C V Y F L E P Q N G M F G V G Y V Y G R D D D R R F G F F C R S A L E F L L Q S G S S P N I I H C U D W S S A P V A W L H K E N Y A K S S L A N A R V V F T I H N L E SEQ. ID. No. 6 SSI Sequence used by 3DPSSM for threading

Secondary Structure Calculated Number of Groups 349 Number of Atoms 2708 Number of Bonds 2791 Number of H-Bonds 237 Number of Helices 20 Number of Strands 17 Number of Turns 30 SEQ. ID. No. 7 SSIIa Sequence utilized by 3DPSSM

Secondary Structure Calculated Number of Groups 358 Number of Atoms 2802 Number of Bonds 2885 Number of H-Bonds 246 Number of Helices 22 Number of Strands 17 Number of Turns 30 SEQ. ID. No. 8 SSIIB- Sequence used by 3DPSSM for threading

SecondaryStructure Calculated Number of Groups 361 Number of Atoms 2888 Number of Bonds 3012 Number of H-Bonds 252 Number of Helices 22 Number of Strands 17 Number of Turns 31 SEQ. ID. No. 9 GBSS GBSS Sequence used by 3D-PSSM

SecondaryStructure Calculated Number of Groups 361 Number of Atoms 2805 Number of Bonds 2877 Number of H-Bonds 252 Number of Helices 21 Number of Strands 17 Number of Turns 30 SEQ. ID. No. 10 Du I DuI sequence used by 3D-PSSM Note: Residue numbered as 37 (listed below) is actually amino acid residue number 1238 in Du1 protein sequence

[0373] TABLE III % align- ENZYME Seq. ID No. Alignment with Pfam 00534 (Glycosyl transferase, Group 1 domain) ment GBSS Seq. Id. query: 378 NKEALQAEVGLPVDRNIPLVAFIGRLEEQKGPDVMAAAIPQLME-MVEDVQIVLLGTGKK 436 91.3 No.11 (query) Seq. Id. Sbjct: 1 DREEIRKKLGIKEEKKI--ILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEE 58 No.12 (snjct) Query: 437 KFERMLMSAEEKFPGKVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTP 496 Sbjct: 59 EDELKLLALKLGLEDNVIFLGFVPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLP 118 Query: 497 CACASTGGLVDTIIEGKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIK 545 Sbjct: 119 VIATDVGGIPEIVKDGETGL----------LVEPGDVEALAEAIEKLLK 157 SSI Seq. Id. Query: 441 LPIRPDVPLIGFIGRLDYQKGID-LIQLI--IPDLMREDVQFVMLGSGDPELEDWMRSTE 497 75 No.13 (query) Seq. Id. Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 No.14-(snjct) Query: 498 SIFKDKFRGWVGF-SVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGGL 556 Sbjct: 69 LGLEDNVI-FLGFVPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGGI 127 Query: 557 RDTVENFNPFGENG 570 Sbjct: 128 PEIVKD----GETG 137 SSIIa Seq. Id. Query: 540 LEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIA---GQDVQLVMLGTGRADLERMLQHLE 596 84.3 No.15 (query) Seq. Id. Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 No.16 (snjct) Query: 597 REHPNKVRGWVGFSVPMAHRIT--AGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 654 Sbjct: 69 LGLEDNVI-FLGF-VPDEDLPELYKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGG 126 Query: 655 LRDTVAPFDPFGDAGLGWTFDRAEANKLIEALR 687 Sbjct: 127 IPEIVKDGET------GLLVEPGDVEALAEAIE 153 SSIIb Seq. Id. Query: 506 LQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIA---GQDVQLVMLGTGRADLEDMLRRFE 562 87.2 No.17 (query) Seq. Id. Sbjct: 9 LGIKEEKKIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALK 68 No.18 (snjct) Query: 563 SEHSDKVRAWVGFS----VPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAV 618 Sbjct: 69 LGLEDNVI-FLGFVPDEDLPELYKS---ADVFVLPSRYEGFGIVLLEAMACGLPVIATDV 124 Query: 619 GGLRDTVAP------FDPFNDTGLGWTFDRAEAN 646 Sbjct: 125 GGIPEIVKDGETGLLVEPGDVEALAEAIEKLLKD 158 DuI Seq. Id. Query: 1478 PVVGIVTRLTAQKGIHLIKHAIHRTLERNGQVVLLGSAPDSRIQADFVNLANTLHGVNHG 1537 70.3 No.19 (query) Seq. Id. Sbjct: 16 KIILFVGRLLPEKGIDLLIEAFKKLKKQLNPNLKLVIVGDGEEEDELKLLALKLGLEDNV 75 No.20 (snjct) Query: 1538 QVRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTQLVAMRYGTIPIVRKTGGLFDTVFD 1597 Sbjct: 76 IFLGFVPDEDLPEL--YKSADVFVLPSRYEGFGIVLLEAMACGLPVIATDVGGIPEIVKD 133 Query: 1598 VDN 1600 Sbjct: 134 GET 136

[0374] TABLE IIIa PIR Multiple Alignment for “GLYTR” Domain of Maize SS enzymes Enzyme Seq (res. # of Id the start) No CLUSTAL W (1.8) multiple sequence alignment SSIIa-540  21 -----------EVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIAG--QDVQLVMLGTG-----RADLERMLQHLEREHPNKVRGWVGFS VPMAHRITAGADVLVMPSFEPCGLNQLYAMAYGTVPVVHAVGGLRDTVAPFDP-FGDAGLGWTFDRAEANKLIEALR---- SSIIb-506  22 ----------LQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIAG--QDVQLVMLGTG-----RADLEDMLRRFESEHSDKVRAWVGFS VPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGGLRDTAPFDP-FNDTGLGWTFDRAEAN-----------   SSI-441  23 ----------LPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLMR--EDVQFVMLGSG-----DPELEDWMRSTESIKDKFRGWVGFSV PVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGGLRDTVENFNP-FGENG----------------------  GBSS-378  24 NKEALQAEVGLPVDRNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTG-----KKKFERMLMSAEEKFPGKVRAVVKFN AALANHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIEGKTGFEMGRLSVDCNVVEPADVKKVATTLC   Dul-1478 25 -----------------PVVGIVTRLTAQKGIHLIKHAIHRTLE--RNGQVVLLGSAPDS RIQADFVNLANTHGVNHGQVRLSLTYD                  *::.::**   *** .::   :       .: *.*:**:.        .:      .    .:.*  :. . EPLSHLIYAGSDFILVPSIFEPCGTQLVAMR YGTIPIVRKTGGLFDTVFDVDN--------------------------- ::* * **.*.: :.* ****** ** .*   ***      .*** **:   .

[0375] TABLE IIIb PIR Multiple Alignment of SSI and SSII enzymes SEQ.ID. ENZYME CLUSTAL W (1.8) multiple sequence alignment No SSIIA.     MSSAAVSSSSSTFFLALASASPGGRRRARVGSSP---FHTGASLSFAFWAPPSPPRAPRD 26          SSIIB.     -MPGAISSSSSAFLLPVASSSPR-RRRGSVGAALRSYGYSGAELR-LHWARRGPPQD--G 27          SSI. --MATPSAVGAACLLLARAAWP-----AAVG-----------DR-----ARPRRLQR--- 29                  .: *: .:: :*   :: *     . **           .      *     : SSIIA.     AALVRAEAEAGGKDAPPERSGDAARLPRARRNAVSKRRDPLQPVGRYGSATGNTARTGAA 26 (cont.d) SSIIB.     AASVRAAAAPAGGESEEAAKSSSSSQAGAVQGSTAKAVDSASPPNPLTSAP---KQSQSA 27          SSI. -VLRRRCVAELSREGPAPRPLPPALLA------P-----PLVP--------------------- 29                .  *  .   . :.       .:  .            .  * SSIIA.     SCQNAALADVEIKSIVAAPPTSIVKFPAPGYRMILPSGDIAPETVLPAPKPLHESPAVDG 26 (cont.d) SSIB.     AMQNG------------------------------TSGGSSASTAAPVSGPKADHPSAPV 27          SSI. ---------------------------------------G-FLAPPAEPTGEPASTPPPVP- 29                                                     *   . .. *.  *    *.. SSIIA.     DSNGIAPPTVEPLVQEATWDFKKYIGFDEPDEAKDDSRVGADDAGSFEHYG-DNDSGPLA 26 (cont.d) SSIIB.     TKREIDASAVKPEPAGDDARPVESIGIAEPVDAKADAAPATDAAASAPYDREDNEPGPLA 27          SSI. -DAGLGDLGLEPE------------GIAEG--SIDNTVVVASEQDSEIVVGKEQARAKVT 29                .  :    ::*             *: *   :  ::   :.   *      ::  . :: SSIIA.     GENVMNVIVVAAECSPWCKTGGLGDVVGALPKALARRGHRVMVVVPRYG------DYVEA 26 (cont.d) SSIIB.     GPNVMNVVVVASECAPFCKTGGLGDVVGALPKALARRGHRVMVVIPRYG------EYAEA 27          SSI. ----QSIVFVTGEASPYAKSGGLGDVCGSLPVALAARGHRVMVVMPRYLNGTSDKNYANA 29                    .::.*:.*.:*:.*:****** *:** *** ********:***      :*.:* SSIIA.     FDMGIRKYYKAAGQDLEVNYFHAFIDGVDFVFIDAPLFRHRQDDIYG---GSRQEIMKRM SSIIB.     RDLGVRRRYKVAGQDSEVTYFHSYIDGVDFVFVEAPPFRHRHNNIYG---GERLDILKRM SSI. FYTEKHIRIPCFGGEHEVTFFHEYRDSVDWVFVDHPSY-HRPGNLYGDKFGAFGDNQFRY           :      * : **.:** : *.**:**:: * : ** .::**   *   :   * SSIIA.     ILFCKVAVEVPWHVPCGGVCYGDGNLVFIANDWHTALLPVYLKAYYRDHGLMQYTRSVLV 26 (cont.d) SSIIB.     ILFCKAAVEVPWYAPCGGTVYGDGNLVFIANDWHTALLPVYLKAYYRDNGLMQYARSVLV 27          SSI. TLLCYAACEAPLILELGGYIYG-QNCMFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILV 29                *:* .* *.*     **  **  * :*:.****::*:** * * **  *: : :**:** SSIIA.     IHNIAHQGRGPVDEFPYMDLP------EHYLQHFELYDPVG-GEHANIFAAGLKMADRV 26 (cont.d) SSIIB.     IHNIAHQGRGPVDDFVNFDLP------EHYIDHFKLYDNIG-GDHSNVFAAGLKTADRV 27          SSI. IHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHALDKGEAVNFLKGAVVTADRI 29               ***:****  *.. :  :.**       *  : .:   . :. *:  *.: ..: ***: SSIIA.     VTVSRGYLWELKTVEGGWGLHDIIRSNDWKINGIVNGIDHQEWNPKVDVHLRSDGYTNYS 26 (cont.d) SSIIB.     VTVSNGYMWELKTSEGGWGLHDIINQNDWKLQGIVNGIDMSEWNPAVDVHLHSDDYTNYT 27          SSI.     VTVSKGYSWEVTTAEGGQGLNELLSSRKSVLNGIVNGIDINDWNPATDKCIP----CHYS 29              ****.** **:.* *** **:::: ...  ::******* .:*** .*   :     :*: SIIA.     LETLDAGKRQCKAALQRELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIAGQDVQLV 26 (cont.d) SSIIB.     FETLDTGKRQCKAALQRQLGLQVRDDVPLIGFIGRLDHQKGVDIIADAIHWIAGQDVQLV 27          SSI.     VDDLS-GKAKCKGALQKELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLMREDVQFV 29               : *. ** :**.***::*** :* ****:******* ***:*:*   :  :  :***:*     MLGTGRADLERMLQHLEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLY 26 (cont.d) SSIIA.     MLGTGRADLEDMLRRFESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLY 27          SSIIB.     MLGSGDPELEDWMRSTESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLY 29          SSI.     ***:* .:**  ::  *  . *.*. *******::******.*:*:************** SSIIA.     AMAYGTVPVVHAVGGLRDTVAPFDPFGDAG---LGWTFDRAEANKLIEALRHCLDTYRKY 26 (cont.d) SSIIB.     AMAYGTVPVVHAVGGLRDTVAPFDPFNDTG---LGWTFDRAEANRMIDALSHCLTTYRNY 27          SSI.     AMQYGTVPVVHATGGLRDTVENFNPFGENGEQGTGWAFAPLTTENMFVDIANCN------ 29              ** *********.*******  *:**.: *    ::.::  : :* SSIIA.     GESWKSLQARGMSQDLSWDHAAELYEDVLVKAKYQW 26 (cont.d) SSIIB.     KESWRACRARGMAEDLSWDHAAVLYEDVLVKAKYQW 27          SSI. ------IYIQGTQVLLGRANEARHVKRLHVGPCR-- 29         

[0376] TABLE IV Possible, but not limited to Amino acid Sequences for Some of the Proposed Fusion Proteins A. GBSS (61-300) + Du1 (1201-1674) SEQ.ID. No. 30 RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS VVSEIKMGDG YETVRFFRCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAI EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN WMKAGILEAD RVLTVSPYYA EELISGIARG CELDNIMRLT GITGIVNGMD VSEWDPSRDK GGIYDNRNGL DYHIPVFGSI AKEPPMHIVH IAVEMAPIAK VGGLGDVVTS LSRAVQDLGH NVEVILPKYG CLNLSNVKNL QIHQSFSWGG SEINVWRGLV EGLCVYFLEP QNGMFGVGYV YGRDDDRRFG FFCRSALEFL LQSGSSPNII HCHDWSSAPv AWLUKENYAK SSLANARVVF TIHNLEFGAH HIGKAMRYCD KATTVSNTYS KEVSGHGAIV PHLGKFYGIL NGIDPDIWDP YNDNFIPVHY TCENVVEGKR AAKRALQQKF GLQQIDVPVV GIVTRLTAQK GIHLIKHAIH RTLERNGQVV LLGSAPDSRI QADFVNLANT LHGVNHGQVR LSLTYDEPLS HLIYAGSDFI LVPSIFEPCG LTQLVAMRYG TIPIVRKTGG LFDTVFDVDN DKERARDRGL EPNGFSFDGA DSNGVDYALN RAISAWFDAR SWFHSLCKRV MEQDWSWNRP ALDYIELYRS ASKL B. GBSS (61-300) + SSI (400-622) SEQ.ID. No. 31 RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS VVSEIKMGDG YETVRFFECY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN KATTVSNTYS KEVSGHGAIV PHLGKFYGIL NGIDPDIWDP NGIDINDWNP ATDKCIPCHY SVDDLSGKAK CKGALQKELG LPIRPDVPLI GFIGRLDYQK GIDLIQLIIP DLMREDVQFV MLGSGDPELE DWMRSTESIF KDKFRGWVGF SVPVSHRITA GCDILLMPSR FEPCGLNQLY AMQYGTVPVV HATGGLRDTV ENFNPFGENG EQGTGWAFAp LTTENMFVDI ANCNIYIQGT QVLLGRANEA RHVKRLHVGP CR C. GBSS (61-300) + SSIIa (481-732) SEQ.ID. No. 32 RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTs VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN DIIRSNDWKI NGIVNGIDHQ EWNPKVDVHL RSDGYTNYSL ETLDAGKRQC KAALQRELGL EVRDDVPLLG FIGRLDGQKG VDIIGDAMPW IAGQDVQLVM LGTGRADLER MLQHLEREHP NKVRGWVGFS VPMAHRITAG ADVLVMPSRF EPCGLNQLYA MAYGTVPVVH AVGGLRDTVA PFDPFGDAGL GWTFDRAEAN KLIEALRUCL DTYRKYGESW KSLQARGMSQ DLSWDHAAEL YEDVLVKAKY QW D. GBSS (61-300) + SSIIb (481-698) SEQ.ID. No. 33 RRGGRFPSLV VCASAGMNVV FVGAEMAPWS KTGGLGDVLG GLPPAMAANG HRVMVVSPRY DQYKDAWDTS VVSEIKMGDG YETVRFFHCY KRGVDRVFVD HPLFLERVWG KTEEKIYGPV AGTDYRDNQL RFSLLCQAAL EAPRILSLNN NPYFSGPYGE DVVFVCNDWH TGPLSCYLKS NYQSHGIYRD AKTAFCIHNI SYQGRFAFSD YPELNLPERF KSSFDFIDGY EKPVEGRKIN YTNYTFETLD TGKRQCKAAL QRQLGLQVPD DVPLIGFIGR LDHQKGVDII ADAIHWIAGQ DVQLVMLGTG RADLEDMLRR FESEHSDKVR AWVGFSVPLA HRITAGADIL LMPSRFEPCG LNQLYAMAYG TVPVVHAVGG LRDTVAPFDP FNDTGLGWTF DRAEANRMID ALSHCLTTYR NYKESWRACR ARGMAEDLSW DHAAVLYEDV LVKAKYQW

[0377] Amino acid sequence of maize granule bound starch synthase (GBSS) Accession numbers: EMBL; X03935; E276624; -;                    PIR; S07314; S07314;                    MAIZEDB; 15806 SEQ.ID. No. 34 1 M A A L A T S Q L V A T R A G L G V P D A S T F R R G A A Q 31 G L R G A R A S A A A D T L S M R T S A R A A P R H Q Q Q A 61 R R G G R F P S L V V C A S A G M N V V F V G A E M A P W S 91 K T G G L G D V L G G L P P A M A A N G H R V M V V S P R Y 121 D Q Y K D A W D T S V V S E I K M G D G Y E T V R F F H C Y 151 K R G V D R V F V D H P L F L E R V W G K T E E K I Y G P V 181 A G T D Y R D N Q L R F S L L C Q A A L E A P R I L S L N N 211 N P Y F S G P Y G E D V V F V C N D W H T G P L S C Y L K S 241 N Y Q S H G I Y R D A K T A F C I H N I S Y Q G R F A F S D 271 Y P E L N L P E R F K S S F D F I D G Y E K P V E G R K I N 301 W M K A G I L E A D R V L T V S P Y Y A E E L I S G I A R G 331 C E L D N I M R L T G I T G I V N G M D V S E W D P S R D K 361 Y I A V K Y D V S T A V E A K A L N K E A L Q A E V G L P V 391 D R N I P L V A F I G R L E E Q K G P D V M A A A I P Q L M 421 E M V E D V Q I V L L G T G K K K F E R M L M S A E E K F P 451 G K V R A V V K F N A A L A H H I M A G A D V L A V T S R F 481 E P C G L I Q L Q G M R Y G T P C A C A S T G G L V D T I I 511 E G K T G F H M G R L S V D C N V V E P A D V K K V A T T L 541 Q R A I K V V G T P A Y E E M V R N C M I Q D L S W K G P A 571 K N W E N V L L S L G V A G G E P G V E G E E I A P L A K E 601 N V A A P

[0378] TABLE VII Maize Granule bound starch synthase (GBSS) Aligmnents with other similar proteins-Transit Peptide SEQ Accession a.a a.a. Id.No. Number # Sequence # 35 maize GBSS 1 MAALATSQLVATRAGLGVPD----ASTF--XXXXXXXXXXXXXXXXXDTLSMRT---S-- 49 36   136757 1 MAALAT8QLVATRAGLGVPD----ASTF--RRGAAQGLRGARASAAADTLSMRT---S-- 49 37  2833385 1 MSTLATSQLVATHAGLGVPD----ASMFRRGGVQGLRAAARASAAAGDALSMRT---SAC 53 38   136758 1 MSALTTSQLATSATGFGIADRSAPSSLL--RHGFQGLKPRSPAGGDATSLSVTT---S-- 53 39  2833382 1 MSALTTSQLATSATGFGIADRSAPSSLL--REGFQGLKPRSPAGGDATSLSVTT---S-- 53 40   297424 1 MSALTTSQLATSATGFGIADRSAPSSLL--RHGFQGLKPRSPAGGDATSLSVTT---D-- 53 41  7798551 1 MSALTTSQLATSATGFGIADRSAPSSLL--RHGFQGLKPRSPAGGDATSLSVTT---S-- 53 42    82478 1 MSALTTSQLATSATGFGIADRSAPSSLL--RHGFQGLKPRSPAGGDATSLSVTT---S-- 53 43   297422 1 MSALTTSQLATSATGFGIADRSAPSSLL--RHGFQGLKPRSPAGGDASSLSVTT---S-- 53 44   136755 1 MAALATSQLATSGTVLGVTD----------RFRRPGFQGLRPRNPADAALGMRT---I-- 45 45 18652407 1 MAALATSQLATSGTVLGVTD----------RFRRPGFQGLRPRNPADAALGMRT---I-- 45 46  4760582 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRSPADAPLGMRTTGAS-- 48 47 11037536 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRSPADAPLGMRTTGAS-- 48 48  6624287 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRNPADAALVMRT---I-- 45 49  6624283 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRSPADAPLGMRTTGAS-- 48 50  4760584 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRSPADAALGMRT---V-- 45 51  6318538 1 MAALVTSQLATSGAVLGITD----------RFRRAGFQGVRPRSPADAPLGMRTVGAS-- 48 52  6318540 1 MAALVTSQLATSATVLGITD----------RFRRAGFQGVRPRSPADAPLGMRTVGAS-- 48 53  6624285 1 MAALVTSQLATSGTVLSVTD----------RFRRPGFQGLRPRNPADAALGMRT---V-- 45 54  6624281 1 MAALVTSQLATSGTVLSVTD----------RFRRPGFQGLRPRNPADAALGMRTVG-A-- 47 55  4760580 1 MAALVTSQLATSGTVLSVTD----------RFRRPGFQGLRPRNPADAALGMRTVG-A-- 47 56   136765 1 MAALVTSQLATSGTVLSVTD----------RFRRPGFQGLRPRNPADAALGMRTVG-A-- 47 57  4588609 1 MAALVTSQLATSGTVLGITD----------RFRRAGFQGVRPRSPADAALGMRT---V-- 45 58  6136121 49                                                DKLQMRN---N-- 56 59 15637079 48                                                DMLQLRT---S-- 55 60  2833388 50                                                DKLQMKT---Q-- 57 35 (cont.d) GBSS 50 -XXXXXXXXXXXXXGG--RFPSLVVCA--S-AGMNVVFVGAEMAPWSKTXXXXXXXXXXP 103 36 (cont.d)   136757 50 -ARAAPRHQQQARRCG--RFPSLVVCA--S-AGMNVVFVGAEMAPWSKTGGLGDVLGGLP 103 37 (cont.d)  2833385 54 PAPRQQPAARRGGRGG--RFPSLVVCA--T-AGMNVVFVGAEMAPWSKTGGLGDVLGGLP 108 38 (cont.d)   136758 54 -APATPKQQRSVQRGSR-RFPSVVVYA--TGAGMNVVFVGAEMAPWSKTGGLGDVLGGLP 109 39 (cont d)  2833382 54 -ARATPKQQRSVQRGSR-RFPSVVVYA--TGAGNNVVFVGAEMAPWSKTGGLGDVLGGLP 109 40 (cont.d)   297424 54 -ARATPKQQRSVQRGSR-RFPSVVVYA--TGAGNNVVFVGAEMAPWSKTGGLGDVLGGLP 109 41 (cont.d)  7798551 54 -APATPKQQRSVQRGSR-RFPSVVVYA--TGAGNNVVFVGAEMAPWSKTGGLGDVLGGLP 109 42 (cont.d)    82478 54 -ARATPKQQRSVQRGSR-RFPSVVVYA--TGAGMNVVFVGAEMAPWSKTGGLGDVLGGLP 109 43 (cont.d)   297422 54 -ARATPKQQRSVQRGSR-RFPSVVVYA--TGAGMNVVFVGAEMAPWSKTGGLGDVLGGLP 109 44 (cont d)   136755 46 -GASAAPKQSRKAHRGSRRCLSVVVRA--TGSGMNLVFVGAEMAPWSKTGGLGDVLGGLP 102 45 (cont.d) 18652407 46 -GASAAPKQSRKAHRGSRRCLSVVVRA--TGSGMNLVFVGAEMAPWSKTGGLGDVLGGLP 102 46 (cont.d)  4760582 49 -AAPKQQSRKAHRGTR--RCLSMVVRATGS-AGMNLVFVGAEMAPWSKTGGLGDVLGGLP 104 47 (cont.d) 11037536 49 -AAPKQQSRKAHRGTR--RCLSMVVRATGS-AGMNLVFVGAEMAPWSKTGGLGDVLGGLP 104 48 (cont.d)  6624287 46 -GASAAPKQSRKAHRGSRRCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 49 (cont.d)  6624283 49 -AAPKQQSRKAHRGTR--RCLSMVVRATGS-AGMNLVFVGAEMAPWSKTGGLGDVLGGLP 104 50 (cont.d)  4760584 46 -GASAAPTQSRKAHRGTRRCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 51 (cont.d)  6318538 49 -AAPKQQSRKAHRGTR--RCLSVVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 104 52 (cont.d)  6318540 49 -AAPKQQSRKAHRGTR--RCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 104 53 (cont.d) 17736918 46                             --S-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 33 54 (cont.d)  6624285 46 -GASAAPKQSRKPHRGNRRCLSMVVRATGS-GGMNLVFVCAEMAPW5KTGGLGDVLGGLP 103 55 (cont.d)  6624281 48 -SAAPKQSRKPHRFDR--RCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 56 (cont.d)  4760580 48 -SAAPKQSRKPHRFDR-RCLSMVVR ATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 59 (cont.d)   136765 48 -SAAPKQSRKPHRFDR--RCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 57 (cont.d)  4588609 46 -GASAAPTQSRKAHRGTRRCLSMVVRATGS-GGMNLVFVGAEMAPWSKTGGLGDVLGGLP 103 62 (cont.d)  4588607 36                           A--D-AALGIRTVGASAAP--KQSRKPHRGNRRC 64 58 (cont.d)  6136121 57 -AKQSRSLVKKTDNGS--PLGK-IICG--T--GMNLVFVLAEVGPWSKTGGLGDVVGGLP 108 59 (cont.d) 15637079 56 --AKKPSKNGRENEGG--MAAGTIVCK--Q-QGMNLVFVGCEVGPWCKTGGLGDVLGGLP 108 63 (cont.d)  3832512 75                        IVCG--N--GMNLVFVGAEVGPWSKTGGLGDVLGGLP 107 64 (cont.d)  2833381 75                        IVCK--Q-QGMNLVFVGCEEGPWCKTGGLGDVLGGLP 108 65 (cont.d) 12003285 73                          CE--T-SGMTLIFVSAECGPWSKTGGLGDVVGGLP 104 66 (cont.d)   228210 75                        IVCG--K--GMNLIFVGTEVGPWSKTGGLGDVLGGLP 107 67 (cont.d) 15626365 82                        IIVC-----GMNLIFVGTEVAPWSKTGGLGDVLGGLP 113 68 (cont.d)   267196 75                        IVCG--K--GMNLIFVGTEVGPWSKTGGLGDVLGGLP 107 60 (cont.d)  2833388 58 ---SKAVKKVSATGNG--RPAAKIICG--H--GMNLIFVGAEVGPWSKTGGLGDVLGGLP 108 69 (cont.d)   602594 75                        IVCG--K--GMNLIFVGTEVGPWSKTGGLGDVLGGLP 107 70 (cont.d) 15223331 78                        IVC---E-KGMSVIFIGAEVGPWSKTGGLGDVLGGLP 110 71 (cont.d)  5441242 79                                 GMNLIFVGAEVAPWSKTGGLGDVLGGLP 106 72 (cont.d) 18139611 75                        IVC---S-AGMTIIFIATECHPWCKTGGLGDVLGGLP 107 73 (cont.d)  2833383 73                        IVC------GMSLVFVGAEVGPWSKTGGLGDVLGGLP 103 74 (cont.d)  6492245 61                 --RTPAPIVC---S-TGMPIIFVATEVHPWCKTGGLGDVVGGLP 98

[0379] TABLE VIII Maize (GBSS) “GLASS” Domain and it's Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)            “GLASS” Sequence            (ending) # 75 MAIZE-GESS 104 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 163 76   136757 104 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 163 77  2833385 109 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 168 78   136758 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 79  2833382 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 80   297424 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 81  7798551 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 82    82478 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 83   297422 110 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 169 84   136755 103 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 162 85 18652407 103 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 162 86  4760582 105 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 164 87 11037536 105 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 164 88  6624287 104 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 163 89  6624283 105 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 164 90  4760584 104 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 163 91  6318538 105 PAMAANGRRVMVISPRYDQYKDAWDTSVVSEIKVADEYERVRYFHCFKRGVDRVFVDHPC 164 92  6318540 105 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 164 93 17736918 34 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 93 94  6624285 104 AAMAANGHRVMVISPRYDQYKDAWDTSVISEIKVVDRYERVRYFHCYKRGVDRVFVDHPC 163 95  6624281 104 AAMAANGHRVMVISPRYDQYKDAWDTSVISEIKVVDRYERVRYFHCYKRGVDRVFVDHPC 163 96  4760580 104 AAMAANGHRVMVISPRYDQYKDAWDTSVISEIKVVDRYERVRYFHCYKRGVDRVFVDHPC 163 97   136765 104 AAMAANGHRVMVISPRYDQYKDAWDTSVISEIKVVDRYERVRYFHCYKRGVDRVFVDHPC 163 98  4588609 104 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 163 99  4588607 65 LSMVANGHRVMVISPRYDQYKDAWDTSVISEIKVVDRYERVRYFHCYKRGVDRVFVDHPC 124 100  6136121 109 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 168 101 15637079 109 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 168 102  3832512 108 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 167 103  2833381 109 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 168 104 12003285 105 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 164 105   228210 108 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 167 106 15626365 114 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 173 107   267196 108 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 167 108  2833388 109 PAMAANGHRVMVVSPRYDQYKDAWDTSVVSEIKMGDGYETVRFFHCYKRGVDRVFVDHPL 168 109   602594 108 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 167 110 15223331 111 PALAARGHRVMTVCPRYDQYKDAWDTCVWELQVGDRIEPVRFFHSYKRGVDRVFVDHPM 170 111  5441242 107 SALAEHGHRVMTVSPRYDQYKDAWDTNVTVEVKVADRIETVRFFHCYKQGVDRVFVDHPC 166 112 18139611 108 PALAAMGHRVMTIVPRYDQYKDAWDTNVLVEVNIGDRTETVRFFHCYKRGVDRVFVDHPM 167 113  2833383 104 PVLAGNGHRVMTVSPRYDQYKDAWDTNVLVEVKVGDKIETVRFFHCYKRGVDRVFVDHPL 163 114  6492245 99 PALAAMGHRVMTIAPRYDQYKDTWDTNVLVEVIVGDRTETVRFFHCYKRGVDRVFVDHPM 158 115  9587307 12 PAMAANGHRVMTISPRYDQYKDAWDTEVTVELKVGDKTETVRFFHCYKRGVDRVFVDHPM 71 116  9587337 12 PANAANGHRVMTISPRYDQYKDAWDTEVTVELKVGDKIETVRFFHCYKRGVDRVFVDHPL 71 117  9587327 12 PAMAANGHRVMTISPRYDQYKDAWDTEVTVELKVGEKIEFVRFFHCYKRGVDRVFVDHPL 71 118  9587333 12 PANAANGHRVMTVSPRYDQYKDAWDTEVTVELKVGQKIETVRFFHCHKRGVDRVFVDHPL 71 119  9587329 12 PALAANGHRVMTVSPRYDQYKDAWDTNVLVEIEVGGKIETVRFFHCYKRGVDRVFVDHPL 71 120  9587325 12 PAMAANGHRVMTISPRYDQYKDAWDTEVTVELNVGEKTETVRFFECYKRGVDRVFVDHPL 71 75 MAIZE-GESS 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 76   136757 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 77  2833385 169 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 223 78   136758 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 224 79  2833382 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 224 80   297424 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 224 81  7798551 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 224 82    82478 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 224 83   297422 170 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQ---EAPRILSLNNNPYFSGPY----- 221 84   136755 163 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 217 85 18652407 163 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 217 86  4760582 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 87 11037536 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 88  6624287 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 89  6624283 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 90  4760584 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 91  6318538 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 92  6318540 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 93 17736918 94 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 148 94  6624285 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 95  6624281 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 96  4760580 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 97   136765 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPYAMLCR 223 98  4588609 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 99  4588607 125 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 179 100  6136121 169 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 223 101 15637079 169 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 223 102  3832512 168 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 222 103  2833381 169 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 223 104 12003285 165 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 219 105   228210 168 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 222 106 15626365 174 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 228 107   267196 168 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 222 108  2833388 169 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 223 109   602594 168 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 222 110 15223331 171 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 225 111  5441242 167 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 221 112 18139611 168 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 222 113  2833383 164 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 218 114  6492245 159 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 213 115  9587307 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 116  9587337 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 117  9587327 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 118  9587333 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 119  9587329 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 120  9587325 72 FLERVWGKTEEKIYGPVAGTDYRDNQLRFSLLCQAALEAPRILSLNNNPYFSGPY----- 126 75 MAIZE-GESS 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 76   136757 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 77  2833385 224 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 277 78   136758 225 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 278 79  2833382 225 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 278 80   297424 225 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 278 81  7798551 225 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 278 82    82478 225 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 278 83   297422 222 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 275 84   136755 218 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 271 85 18652407 218 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 271 86  4760582 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 87 11037536 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 88  6624287 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 89  6624283 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 90  4760584 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 91  6318538 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 92  6318540 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 93 17736918 149 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 202 94  6624285 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 95  6624281 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 96  4760580 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 97   136765 224 AVPRRAGEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 283 98  4588609 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 99  4588607 180 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 233 100  6136121 224 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 277 101 15637079 224 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 277 102  3832512 223 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 276 103  2833381 224 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 277 104 12003285 220 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 273 105   228210 223 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 276 106 15626365 229 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 282 107   267196 223 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 276 108  2833388 224 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 277 109   602594 223 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 276 110 15223331 226 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 279 111  5441242 222 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 275 112 18139611 223 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 276 113  2833383 219 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 272 114  6492245 214 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 267 115  9587307 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180 116  9587337 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180 117  9587327 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180 118  9587333 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180 119  9587329 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180 120  9587325 127 ------GEDVVFVCNDWHTGPLSCYLKSNYQSHGIYRDAKTAFCIHNISYQGRFAFSDYP 180

[0380] TABLE IX Maize (GBSS) “LINKR” Domain and it's Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)             “LINKR” Sequence             (ending) # 121 MAIZE GESS 273 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 332 122    136757 273 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 332 123   2833385 278 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 337 124    136758 279 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 338 125   2833382 279 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 338 126    297424 279 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 338 127   7798551 279 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 338 128     82478 279 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 338 129    297422 276 ELNLPERFKSSFDFIDGYEKPVEGRKINWMKAGILEADRVLTVSPYYAEELISGIARGCE 335 130    136755 272 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 331 131 118652407 272 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 331 132   4760582 274 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 333 133  11037536 274 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 333 134   6624287 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 135   6624283 274 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 333 136   4760584 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 137   6318538 274 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 333 138   6318540 274 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 333 139  17736918 203 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 262 140   6624285 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 141   6624281 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 142   4760580 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 143    136765 284 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 343 144   4588609 273 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 332 145   4588607 234 QLNLPDRFKSSFDFIDGYDKPVEGRKINWMKAGILQADKVLTVSPYYAEELISGEARGCE 293 146   6136121 278 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 337 147  15637079 278 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 337 148   3832512 277 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 336 149   2833381 278 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 337 150  12003285 274 KLNLPDQLKSSFDFMDGYEKPVKGRKINWMKAGIIESDRVLTVSPYYANELVSGPDKGVE 333 151    228210 277 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 336 152  15626365 283 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 342 153    267196 277 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 336 154   2833388 278 RLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 337 155    602594 277 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 336 156  15223331 280 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 339 157   5441242 276 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 335 158  18139611 277 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 336 159   2833383 273 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 332 160   6492245 268 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 327 161   9587307 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 162   9587337 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 163   9587327 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 164   9587333 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 165   9587329 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 166   9587325 181 LLNLPDQFKSSFDFFDGYEKPVKGRKINWMKAGILESDRVVTVSPYYAKELVSGPDKGVE 240 121 MAIZE GESS 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 122    136757 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 123   2833385 338 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 396 124    136758 339 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 397 125   2833382 339 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 397 126    297424 339 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 397 127   7798551 339 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 397 128     82478 339 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 397 129    297422 336 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 394 130    136755 332 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 390 131  18652407 332 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 390 132   4760582 334 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 392 133  11037536 334 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 392 134   6624287 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 135    662428 334 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 392 136   4760584 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 137   6318538 334 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 392 138   6318540 334 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 392 139  17736918 263 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 321 140   6624285 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 141   6624281 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 142   4760580 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 143    136765 344 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 402 144   4588609 333 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 391 145   4588607 294 LDNIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 352 146   6136121 338 LDNVIAKTSI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 396 147  15637079 338 LDNHIRDCGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 396 148   3832512 337 LDNIIRSIGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 395 149   2833381 338 LDNHIRDCGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 396 150  12003285 334 LDNILRKCTV-TGIVNGMDTQEWNPATDKYIDNHYDITTDGKPLLKEALQAEVGLPVD 392 151    228210 337 LDSVLRKTCI-TGIVNGMDTQEWNPATDKYIDNHYDITTDGKPLLKEALQAEVGLPVD 395 152  15626365 343 LDNILRRVGV-TGIVNGMDTQEWNPATDKYIDNHYDITTDGKPLLKEALQAEVGLPVD 401 153    267196 337 LDSVLRKTCI-TGIVNGMDTQEWNPATDKYIDNHYDITTDGKPLLKEALQAEVGLPVD 395 154   2833388 338 LDNFIRKTGI-AGIINGMDVQEWNPVTDKYIDIHYDATTVMDAKPLLQAEVGLPVD 396 155    602594 337 LDSVLRKTCI-TGIVNGMDTQEWNPATDKYIDNHYDITTDGKPLLKEALQAEVGLPVD 395 156  15223331 340 LHKYLRMKTV-SGIINGMDVQEWNPSTDKYIDIKYDITTVTDAKPLIKEALQAAVGLPVD 398 157   5441242 336 LDNIIRKTGV-AGIVNGMDIREWSPKTDKFIDIHFDTTSVKEAKFLLQAEVGLPVN 394 158  18139611 337 LDGILRTKPLETGIVNGMDVYEWNPATDQYISVKYDATTVTEARALNKEMLQAEVGLPVD 396 159   2833383 333 LDNIIRSTGI-IGIVNGMDNREWSPQTDRYIDETTVTEAKPLLKGTLQAEIGLPVD 391 160   6492245 328 LDGVLRAKPLETGIVNGMDVVDWNPATDKYISVKYNATAKEILQAEVGLPVD 387 161   9587307 241 LDNIIRKTGI-QFGIVNGMVQEWNPLTDKYTTVKYDASTVADAKPLLKEALQAEVGLPVD 299 162   9587337 241 LDNIIRKTGI-QFGIVNGMVQEWNPLTDKYTTVKYDASTVADAKPLLKEALQAEVGLPVD 299 163   9587327 241 LDNIIRKTGI-QFGIVNGMVQEWNPLTDKYTTVKYDASTVADAKPLLKEALQAEVGLPVD 299 164   9587333 241 LDNIIRKTGI-QFGIVNGMVQEWNPLTDKYTTVKYDASTVADAKPLLKEALQAEVGLPVD 299 167    150549 221   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 57 165   9587329 241   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 299 168  15054954 1   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 57 169  15054970 1   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 57 170  15054956 1   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 57 171  15054960 1   NIMRLTGI-TGIVNGMDVSEWDPSRDKYIAVKYDVSTAVEAKALNKEALQAEVGLPVD 57 166 958732524 1 LDNIIRKTGI-RGIVNGMDVQEWNPLTDKYTIVKYDASTVTDAKPLLKEASQAEVGLFVD 299

[0381] TABLE X Maize (GBSS) “GLYTR” Domain and it's Alignments with other proteins SEQ Accession a.a a.a. Id.No. Number # (start)             “GLYTR” Sequence             (ending) # 172 MAIZE GBSS 392 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 451 173   136757 392 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 451 174  2833385 397 RKIPLVAFIGRLEEQKGPDVMAAAIPQLME--EDVQIVLLGTGKKKFERMLMSAEEKFPG 454 175   136758 398 RKIPLVAFIGRLEEQKGPDVMAAAIPQLMQ--EDVQIVLLGTGKKKFERMLMSAEEKFPG 455 176  2833382 398 RKIPLVAFIGRLEEQKGPDVMAAAIPQLMQ--EDVQIVLLGTGKKKFERMLMSAEEKFPG 455 177   297424 398 RKIPLVAFIGRLEEQKGPDVMAAAIPQLMQ--EDVQIVLLGTGKKKFERMLMSAEEKFPG 455 178  7798551 398 RKIPLVAFIGRLEEQKGPDVMAAAIPQLMQ--EDVQIVLLGTGKKKFERMLMSAEEKFPG 455 179    82478 398 RKIPLIAFIGRLEEQKGPDVMAAAIPELMQ--EDVQIVLLGTGKKKFEKLLKSMEEKYPG 455 180   297422 395 RKVPLIAFIGRLEEQKGPDVMAAAIPELMQ--ENVQIVLLGTGKKKFEKLLKSMEEKYPG 452 181   136755 391 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPG 449 182 18652407 391 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPG 449 183  4760582 393 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPD 451 184 11037536 393 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 451 185  6624287 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPN 450 186  6624283 393 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 451 187  4760584 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 450 188  6318538 393 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 451 189  6318540 393 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 451 190 17736918 322 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 380 191  6624285 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPT 450 192  6624281 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPT 450 193  4760580 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPT 450 194   136765 403 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPT 461 195  4588609 392 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPS 450 196  4588607 353 RKVFLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIILLGTGKKKFEKLLKSMEEKFPT 411 197  6136121 397 KNIPVIGFIGRLEEQKGSDILVAAISKFVGL--DVQIIILGTGKKKFEQQIQELEVLYPD 454 198 15637079 397 RNIPLIGFIGRLEEQKGSDILYAAISKFISM--DVQILILGTGKKKFEQQIEQLEVMYPD 454 199  3832512 396 RNIPVIGFIGRLEEQKGSDILVESIPKFID--QNVQIIVLGTGKKIMEKQIEQLEVTYPG 453 200  2833381 397 RNIPLIGFIGRLEEQKGSDILYAAISKFISM--DVQILILGTGKKKFEQQIEQLEVMYPD 454 201 12003285 393 PNVPLVGFIGRLEEQKGSDILVAALHKFIEM--DVQVVILGTGKKEFEKQIEQLEELYPG 450 202   228210 396 KKIPLIGFIGRLEEQKGSDILVAAIHKFIGL--DVQIVVLGTGKKEFEQEIEQLEVLYPG 453 203 15626365 402 KNVPLIAFIGRLEEQKGSDILVEAIPQFIK--ENVQIVALGTGKKEMEKQLQQLEISYPD 459 204   267196 396 KKIPLIGFIGRLEEQKGSDILVAAIHKFIGL--DVQIVVLGTGKKEFEQEIEQLEVLYPN 453 205  2833388 397 PNVPLIGFIGRLEEQKGSDIFVAAISQLVE--HNVQIVILGTGKKKFEKQIEHLEVLYPD 454 206   602594 396 KKVPLIGFIGRLEEQKGSDILVAAIHKFIGL--DVQIVVLGTGKKEFEQEIEQLEVLYPN 453 207 15223331 399 RDVPVIGFIGRLEEQKGSDILVEAISKFMGL--NVQMVILGTGKKKMEAQILELEEKFFG 456 208  5441242 395 RDIPLIGFIGRLEEQKGSDILVEAIPKFID--QNVQIIILGTGKKSMEKQIEQLEEIYPE 452 209 18139611 397 SSIPLIVFVGRLEEQKGSDILIAAIPEFVE--GNVQIIVLGTGKKKMEEELILLEVKYPN 454 210  2833383 392 SSIPLIGFIGRLEEQKGSDILVEAIAKFAD--ENVQIVVLGTGKKIMEKQIEVLEEKYPG 449 211  6492245 388 SSIFVIVFIGRLEEQKGSDILIAAIPEFLE--ENVQIIVLGTGKKKMEEELMLLEAKYPQ 445 212  9587307 300 RDIPVIGFIGRLEE 313 213  9587337 300 RDIFVIGFIGRLEE 313 214  9587327 300 KDIPVIGFIGRLEE 313 215  9587333 300 KMIPVIGFIGRLEE 313 216 15054922 58 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFEPMLMSAEEKFFG 117 217  9587329 300 RDIPVIGFIGRLEE 313 218 15054954 58 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 117 219 15054970 58 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMDMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 117 220 15054956 58 PNIPLVAEIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 117 221 15054960 58 RNIPLVAFIGRLEEQKGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPG 117 222  9587325 300 RDIPVIGFIGRLEE 313 172 MAIZE GBSS 452 KVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 511 173   136757 452 KVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 511 174  2833385 455 KVRAVVKFNAPLAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 514 175   136758 456 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 515 176  2833382 456 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 515 177   297424 456 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 515 178  7798551 456 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 515 179    82478 456 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 515 180   297422 453 KVRAVVKFNAPLAHLIMAGADVLAVPSRFEPCGLIQLQGMRYGTPCACASTGGLVDTVIE 512 181   136755 450 KVRAVVRFNAPLAHQMMAGADLLAVTSRFEPCGLIQLQGMRYGTPCVCASTGGLVDTIVE 509 182 18652407 450 KVRAVVRFNAPLAHQMMAGADLLAVTSRFEPCGLIQLQGMRYGTPCVCASTGGLVDTIVE 509 183  4760582 452 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIME 511 184 11037536 452 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIME 511 185  6624287 451 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 186  6624283 452 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 511 187  4760584 451 KVPAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 188  6318538 452 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 511 189  6318540 452 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 511 190 17736918 381 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 440 191  6624285 451 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 192  6624281 451 KVRAVVRFNAPLAHQNMAGADVIAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 193  4760580 451 KVWAVVRFNAPLAHQNMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 194   136765 462 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 521 195  4588609 451 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 510 196  4588607 412 KVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIVE 471 197  6136121 455 KARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHANRYGTIPICASTGGLVDTVTE 514 198 15637079 455 KARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHANRYGTPCICASTGGLVDTVKE 514 199  3832512 454 KAIGVAKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTGGLVDTVKE 513 200  2833381 455 KARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHAMPYGTPCICASTGGLVDTVKE 514 201 12003285 451 KAVGVAKFNVPLAHKITAGADFMLVPSRFEPCGLIQLHAMPYGTIPICASTGGLVDTVKE 510 202   228210 454 KVKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGGLVDTVKE 513 203 15626365 460 KARGVAKFNVPLAHMMIAGADFILIPSRFEPCGLIQLQAMRYGTVPIVASTGGLVDTVKE 519 204   267196 454 KAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGGLVDTVKE 513 205  2833388 455 KARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPIVASTGGLVDTVKE 514 206   602594 454 KAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGGLVDTVKE 513 207 15223331 457 KAVGVAKFNVPLAHMITAGADFIIVPSRFEPCGLIQLHAMRYGTVPIVASTGGLVDTVKD 516 208  5441242 453 KARGIAKFDGPLAHKIIAGSDFIMIPSRFEPCGLVQLHSMPYGTVPIVSSTGGLVDTVQE 512 209 18139611 455 TARGLAKFNVPLAHMMFAGADFIIVPSRFEPCGLIQLQGMRYGVVPICSSTGGLVDTVKE 514 210  2833383 450 KAIGITKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTGGLVDTVKE 509 211  6492245 446 NARGIAKFNVPLAHMMFAGANFIIVPSRFEPCGLIQLQGMRYGVIPICSSTGGLVDTVSE 505 216 15054922 118 KVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 177 218 15054954 118 KVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACSSTGGLVDTIIE 177 219 15054970 118 KVRAVVKFNAALAHHINAGADVIAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 177 220 15054956 118 KVRAVVKFNAALAHNIMAGADVIAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 177 221 15054960 118 KVRAVVKFNAALAHHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIE 177 172 MAIZE GBSS 512 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVRNCMIQDLSWKGPAK 571 173   136757 512 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVRNCMIQDLSWKGPAK 571 174  2833385 515 GKTGFHMGRLSVDCNVVEPADVKKVATTLKRAIKVVGTPAYEEMVKNCMIQDLSWKGPAK 574 175   136758 516 GKTGFHMGRLSVDCKVVEPSDVKKVAATLKRAIKVGTPAYEEMVVRNCMIQDLSWKGPAK 575 176  2833382 516 GKTGFHMGRLSVNCKVVEPSDVKKVAATLKRAIKVVGTPAYEEMVRNCMNQDLSWKGPAK 575 177   297424 516 GKTGFHMGRLSVDCKVVEPSDVKKVAATLKRAIKVVGTPAYEEMVRNCMNQDLSWKGPAK 575 178  7798551 516 GKTGFHMGRLSVDCKVVEPSDVKKVAATLKRAIKVVGTPAYEEMVRNCMNQDLSWKGPAK 575 179    82478 516 GKTGFHMGRLSVDGKVVEPSDVKKVAATLKRAIKVVGTPAYEEMVRNCMNQDLSWKGPAK 575 180   297422 513 GKTGFHMGRLSVDGKVVEPSDVQKVATTLKRAIKIVGTPAYNEMVRNCNNQDLSWKGPAK 572 181   136755 510 GKTGFHMGRLSVDCNVVEPADVKKVATTLKRAVKVVGTPAYQEMVKNCMIQDLSWKGPAK 569 182 18652407 510 GKTGFHMGRLSVDCNVVEPADVKKVATTLKRAVKVVGTPAYQEMVKNCMIQDLSWKGPAK 569 183  4760582 512 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 571 184 11037536 512 GKTGFHMGHLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 571 185  6624287 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHGMVKNCMIQDLSWKGPAK 570 186  6624283 512 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 571 187  4760584 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 570 188  6318538 512 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 571 189  6318540 512 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 571 190 17736918 441 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 500 191  6624285 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 570 192  6624281 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 570 193  4760580 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 570 194   136765 522 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 581 195  4588609 511 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKFAVKVVGTPAYHEMVKNCMIQDLSWKGPA 569 196  4588607 472 GKTGFHMGRLSVDCNVVEPADVKKVVTTLKRAVKVVGTPAYHEMVKNCMIQDLSWKGPAK 531 197  6136121 515 GFTGFHMGAFNVECATVDPADVQKIATTVERALAAYGSVAYKEMIQNCMAQDLSWKGPAK 574 198 15637079 515 GYTGFHMGAFNVDCETVDPEDVLKVITTVGRALAMYGTLAFTEMIKNCMSQELSWKGPAK 574 199  3832512 514 GYTGFHVGAFSVECEAVDPADVEKLATTVNRALKTYGTQALKEMILNCMAQDFSWKGPAK 573 200  2833381 515 GYTGFHMGAFNVDCETVDPEDVLKVITTVGRALAIYGTLAFTEMIKNCMSQELSWKGPAK 574 201 12003285 511 GFTGFHMGAFNVECDAVDPADVLKIVKTVGRALEVYGTPAFREMINNCMSLDLSWKGPAK 570 202   228210 514 GYTGFHMGAFNVECDVVDPADVLKIVTTVARALAVYGTLAFAEMIKNCMSEELSWKEPAK 573 203 15626365 520 GFTGFHMGSFNVKCDAVDPVDVDAIPKTVTKALGVYGTSAFAEMIKNCMAQELSWKGPAK 579 204   267196 514 GYTGFHMGAFNVECDVVDPADVLKIVTTVARALAVYGTLAFAEMIKNCMSEELSWKEPAK 573 205  2833388 515 GYTGFQMGALVECDKIDSAflVAAIVKTVARALGTYATAALREMILNCMAQDLSWKGPAR 574 206   602594 514 GYTGFHNGAFNVECDVVDPADVLKIVTTVARALAVYGTLAFAEMIKNCMSEELSWKEPAK 573 207 15223331 517 GYTGFHIGRFNVKCEVVDPDDVIATAKAVTRAVAVYGTSAMQEMVKNCMDQDFSWKGPAR 576 208  5441242 513 GFTGFHMGAFNVDCEAIDPADVEKIATTVRRALGTYGTVAMEKIIQNCMAQDFSWKGPAK 572 209 18139611 515 GVTGFHMGLFNVECETVDPVDVTAVASTVKRALKQYNTPAFQEMVQNCMAQDLSWKGPAK 574 210  2833383 510 GYTGFHAGPFDVECEDVDPDDVDKLAATVKRALKTYGTQAMKQIILNCMAQNFSWKKPAK 569 211  6492245 506 GVTGFHMGSFNVEFETVDPADVAAVASNVTRALKQYKTPSFHANVQNCMAQDLSWKGPAK 565 212 15054922 178 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVFNCMIQDLSWKGPAK 237 218 15054954 178 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVPNCMIQDLSWKGPAK 237 219 15054970 178 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVRNCMIQDLSWKGPAK 237 220 15054956 178 GKTGFHMGRFSVDCNVVEPADVKKVATTLQRAIKVVGTPAYEEMVRNCMIQDLSWKGPAK 237 221 15054960 178 GKTGFHMGRLSVDCNVVEPADVKKVATTLQRAIKVVGTPVYEEMVRNCMIQDLSWKGPAK 237

[0382] TABLE XI Maize (GBSS) “CTEND” Domain and it's Alignments with other proteins SEQ Id.No. Accession Number a.a # (start) “CTEND” Sequence (ending) a.a. # 223 Maize GESS 572 NWENVLLSLXXXXXXXXXXXXXXXXLAKENVAAP 605 224   136757 572 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 605 225  2833385 575 NWENVLLSLGVAGGEPGIEGEEIAPLAKENVAAP 608 226   136758 576 NWENVLLGLGVAGSAPGIEGDEIAPLAKENVAAP 609 227  2833382 576 NWENVLLGLGVAGSAPGIEGDEIAPLAKENVAAP 609 228   297424 576 NWENVLLGLGVAGSAPGIEGDEIAPLAKENVAAP 609 229  7798551 576 NWENVLLGLGVAGSAPGIEGDEIAPLAKENVAAP 609 230    82478 576 NWENVLLGLGVAGSAPGIEGDEIAPLAKENVAAP 609 231   297422 573 NWENVLLGLGVAGSEPGVEGEEIAPLAKENVAAP 606 232   136755 570 NWEDVLLELGVEGSEPGIVGEEIAPLAKENVAAP 603 233 18652407 570 NWEDVLLELGVEGSEPGIVGEEIAPLAMENVAAP 603 234  4760582 572 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 605 235 11037536 572 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 605 236  6624287 571 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 604 237  6624283 572 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 605 238  4760584 571 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 604 239  6318538 572 NWEHThLELGVEGSEPGIVGEEIAPLAMENVAAP 605 240  6318540 572 NWEDVLLELGVEGSEPGVIGEEIAPLAMENVAAP 605 241 17736918 501 NWEDVLLELGVEGSEPGVIGEEIAPLANENVAAP 534 242  6624285 571 NWEDVLLELGVEGSEPGIVGEEIAPLALENVAAP 604 243  6624281 571 NWEDVLLELGVEGSEPGIVGEEIAPLALENVAAP 604 244  4760580 571 NWEDVLLELGVEGSEPGIVGEEIAPLALENVAAP 604 245   136765 582 NWEDVLLELGVEGSEPGIVGEEIAPLALENVAAP 615 246  4588607 532 NWEDVLLELGVEGSEPGIVGEEIAPLALENVAAP 565 247  6136121 575 NWEKMLLSLGVSGSEPGVDGEEIAPLAKENVATP 608 248 15637079 575 NWETVLLSLGVAGSEPGVEGDEIAPLAKENVATP 608 249  3832512 574 QWEQALLSLEVAGSEPGIDGEEVAPLAKENVATP 607 250  2833381 575 NWETVLLSLGVAGSEPGVEGEEIAPLAKENVATP 608 251 12003285 571 NWETVLLSLGVAGSEPGVEGDEIAPLAKENVATP 604 252   228210 574 KWETLLLGLGASGSEPGVEGEEIAPLAKENVATP 607 253 15626365 580 KWEEVLLNLGVPDSEPGIDGQEIAPQAKENVATP 613 254   267196 574 KWETLLLGLGASGSEPGVEGEEIAPLAKENVATP 607 255  2833388 575 MWEKMLLDLEVTGSEPGTEGEEIAPLAKENVPTP 608 256   602594 574 KWETLLLGLGASGSEPGVEGEEIAPLAKENVATP 607 257  1522333 577 LWEKVLLSLNVAGSEAGTEGEEIAPLAKENVATP 610 258  5441242 573 QWEKVLFSLDVGRSEAGIEGDEIAPLAKENVATP 606 259 18139611 575 KWEEVLLGLGVEGSQPGIEGEEVAPLAKENVATP 608 260  2833383 570 LWEKALLNLEVTGNVAGIDGDEIAPLAKENVATP 603 261  6492245 566 KWEEALLGLGVEGSQPGIEGEEIAPLAKQNVATP 599 262 15054922 238 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 271 263 15054954 238 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 271 264 15054970 238 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 271 265 15054956 238 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 271 266 15054960 238 NWENVLLSLGVAGGEPGVEGEEIAPLAKENVAAP 271

[0383] TABLE XII Identities of the Accession Numbers used in Table Numbers VIII-XI. Accession Brief Description of sequences Id. producing significant alignments score E-value gi|136757|sp|P04713|UGST MAIZE Granule-bound glycogen [star . . . 1125 0.0 gi|2833385|sp|Q43134|UGST SORBI Granule-bound glycogen [sta . . . 1062 0.0 gi|136758|sp|P19395|UGST ORYSA Granule-bound glycogen [star . . . 959 0.0 gi|2833382|sp|Q42968|UGST ORYGL Granule-bound glycogen [sta . . . 957 0.0 gi|297424|emb|CAA46294.1| (X65183) glycogen (starch) syntha . . . 956 0.0 gi|7798551|gb|AAC61675.2| (AF031162) granule-bound starch s . . . 956 0.0 gi|82478|pir|JQ0703 UDPglucose--starch glucosyltransferase . . . 951 0.0 gi|297422|emb|CAA45472.1| (X64108) starch granule-bound sta . . . 945 0.0 gi|136755|sp|P09842|UGST HORVU Granule-bound glycogen [star . . . 944 0.0 gi|18652407|gb|AAL77109.1|AF474373_6 (AF474373) granule-bou . . . 943 0.0 gi|4760582|dbj|BAA77351.1| (AB019623) starch synthase (GBSS . . . 939 0.0 gi|11037536|gb|AAG27624.1|AF286320_1 (AF286320) granule bou . . . 937 0.0 gi|6624287|dbj|BAA88512.1| (AB029064) starch synthase (GBSS . . . 936 0.0 gi|6624283|dbj|BAA88510.1| (AB029062) starch synthase (GBSS . . . 935 0.0 gi|4760584|dbj|BAA77352.1| (AB019624) starch synthase (GBSS . . . 935 0.0 gi|6318538|gb|AAF06936.1|AF110373_1 (AF110373) granule-boun . . . 932 0.0 gi|6318540|gb|AAF06937.1|AF110374_1 (AF110374) granule-boun . . . 930 0.0 gi|17736918|gb|AAL41028.1| (AF250137) mutant granule bound . . . 929 0.0 gi|6624285|dbj|BAA88511.1| (AB029063) starch synthase (GBSS . . . 926 0.0 gi|6624281|dbj|BAA88509.1| (AB029061) starch synthase (GBSS . . . 922 0.0 gi|4760580|dbj|BAA77350.1| (AB019622) starch synthase (GBSS . . . 921 0.0 gi|136765|sp|P27736|UGST WHEAT Granule-bound glycogen [star . . . 915 0.0 gi|4588609|gb|AAD26156.1|AF113844_1 (AF113844) granule-boun . . . 910 0.0 gi|4588607|gb|AAD26155.1|AF113843_1 (AF113843) granule-boun . . . 889 0.0 gi|6136121|sp|O82627|UGST ANTMA Granule-bound glycogen [sta . . . 773 0.0 gi|15637079|dbj|BAB68126.1| (AB071604) granule-bound starch . . . 771 0.0 gi|3832512|gb|AAC70779.1| (AF097922) granule-bound glycogen . . . 765 0.0 gi|2833381|sp|Q42857|UGST IPOBA Granule-bound glycogen [sta . . . 764 0.0 gi|12003285|gb|AAG43519.1|AF210699_1 (AF210699) granule-bou . . . 762 0.0 gi|228210|prf||1718316A granule-bound starch synthase [Sola . . . 758 0.0 gi|15626365|emb|CAC69955.1| (AJ345045) granule-bound starch . . . 756 0.0 gi|267196|sp|Q00775|UGST SOLTU Granule-bound glycogen [star . . . 754 0.0 gi|2833388|sp|Q43784|UGST MANES Granule-bound glycogen [sta . . . 754 0.0 gi|602594|emb|CAA58220.1| (X83220) starch (bacterial glycog . . . 752 0.0 gi|15223331|ref|NP 174566.1| (NM_103023) starch synthase, p . . . 742 0.0 gi|5441242|dbj|BAA82346.1| (AB029546) granule-bound starch . . . 734 0.0 gi|18139611|gb|AAL58572.1| (AY069940) granule binding starc . . . 729 0.0 gi|2833383|sp|Q43092|UGST PEA Granule-bound glycogen [starc . . . 726 0.0 gi|6492245|gb|AAF14233.1|AF109395_1 (AF109395) granule-boun . . . 716 0.0 gi|9587307|gb|AAF89255.1|AF285980_1 (AF285980) granule-boun . . . 518 e−146 gi|9587337|gb|AAF89270.1|AF285995_1 (AF285995) granule-boun . . . 517 e−145 gi|9587327|gb|AAF89265.1|AF285990_1 (AF285990) granule-boun . . . 514 e−145 gi|9587333|gb|AAF89268.1|AF285993_1 (AF285993) granule-boun . . . 514 e−144 gi|15054922|gb|AAK82769.1|AF292500_1 (AF292500) granule-bou . . . 513 e−144 gi|9587329|gb|AAF89266.1|AF285991_1 (AF285991) granule-boun . . . 513 e−144 gi|15054954|gb|AAK82785.1|AF292516_1 (AF292516) granule-bou . . . 513 e−144 gi|15054970|gb|AAK82793.1|AF292524_1 (AF292524) granule-bou . . . 512 e−144 gi|15054956|gb|AAK82786.1|AF292517_1 (AF292517) granule-bou . . . 512 e−144 gi|15054960|gb|AAK82788.1|AF292519_1 (AF292519) granule-bou . . . 512 e−144 gi|9587325|gb|AAF89264.1|AF285989_1 (AF285989) granule-boun . . . 511 e−144 gi|3493047|gb|AAD02981.1| (AF079261) granule-bound starch s . . . 511 e−144 gi|15054930|gb|AAK82773.1|AF292504_1 (AF292504) granule-bou . . . 511 e−144 gi|9587313|gb|AFF89258.1|AF285983_1 (AF285983) granule-boun . . . 509 e−143 gi|9587352|gb|AAF89276.1|AF286003_1 (AF286003) granule-boun . . . 509 e−143 gi|15054968|gb|AAK82792.1|AF292523_1 (AF292523) granule-bou . . . 509 e−143 gi|9587331|gb|AAF89267.1|AF285992_1 (AF285992) granule-boun . . . 509 e−143 gi|9587323|gb|AAF89263.1|AF285988_1 (AF285988) granule-boun . . . 509 e−143 gi|9587299|gb|AAF89251.1|AF285976_1 (AF285976) granule-boun . . . 507 e−142 gi|15054940|gb|AAK82778.1|AF292509_1 (AF292509) granule-bou . . . 507 e−142 gi|3493043|gb|AAD02979.1| (AF079259) granule-bound starch s . . . 506 e−142 gi|9587305|gb|AAF89254.1|AF285979_1 (AF285979) granule-boun . . . 506 e−142 gi|3493045|gb|AAD02980.1| (AF079260) granule-bound starch s . . . 505 e−142 gi|9587319|gb|AAF89261.1|AF285986_1 (AF285986) granule-boun . . . 504 e−142 gi|9587311|gb|AAF89257.1|AF285982_1 (AF285982) granule-boun . . . 504 e−141 gi|9587343|gb|AAF89273.1|AF285998_1 (AF285998) granule-boun . . . 503 e−141 gi|9587297|gb|AAF89250.1|AF285975_1 (AF285975) granule-boun . . . 503 e−141 gi|15054984|gb|AAK82800.1|AF292531_1 (AF292531) granule-bou . . . 503 e−141 gi|9587339|gb|AAF89271.1|AF285996_1 (AF285996) granule-boun . . . 502 e−141 gi|9587303|gb|AAF89253.1|AF285978_1 (AF285978) granule-boun . . . 501 e−141 gi|15054990|gb|AAK82803.1|AF292534_1 (AF292534) granule-bou . . . 501 e−141 gi|9587317|gb|AAF89260.1|AF285985_1 (AF285985) granule-boun . . . 500 e−140 gi|9587341|gb|AAF89272.1|AF285997_1 (AF285997) granule-boun . . . 500 e−140 gi|9587348|gb|AAF89274.1| (AF286001) granule-bound starch s . . . 499 e−140 gi|9587293|gb|AAF89248.1|AF285973_1 (AF285973) granule-boun . . . 499 e−140 gi|9587335|gb|AAF89269.1|AF285994_1 (AF285994) granule-boun . . . 497 e−139 gi|9587321|gb|AAF89262.1|AF285987_1 (AF285987) granule-boun . . . 497 e−139 gi|9587309|gb|AAF89256.1|AF285981_1 (AF285981) granule-boun . . . 493 e−138 gi|9587301|gb|AAF89252.1|AF285977_1 (AF285977) granule-boun . . . 493 e−138 gi|9587295|gb|AAF89249.1|AF285974_1 (AF285974) granule-boun . . . 492 e−138 gi|3493007|gb|AAD02961.1| (AF079241) granule-bound starch s . . . 489 e−137 gi|3493041|gb|AAD02978.1| (AF079258) granule-bound starch s . . . 489 e−137 gi|3493019|gb|AAD02967.1| (AF079247) granule-bound starch s . . . 488 e−137 gi|3493021|gb|AAD02968.1| (AF079248) granule-bound starch s . . . 488 e−137 gi|3493005|gb|AAD02960.1| (AF079240) granule-bound starch s . . . 488 e−136 gi|3493035|gb|AAD02975.1| (AF079255) granule-bound starch s . . . 487 e−136 gi|3492995|gb|AAD02955.1| (AF079235) granule-bound starch s . . . 487 e−136 gi|3493037|gb|AAD02976.1| (AF079256) granule-bound starch s . . . 487 e−136 gi|3493025|gb|AAD02970.1| (AF079250) granule-bound starch s . . . 486 e−136 gi|3493023|gb|AAD02969.1| (AF079249) granule-bound starch s . . . 486 e−136 gi|16716335|gb|AAC17969.3| (AF026420) granule-bound starch . . . 485 e−136 gi|3493011|gb|AAD02963.1| (AF079243) granule-bound starch s . . . 485 e−136 gi|13377473|gb|AAK20725.1| (AF318769) granule-bound starch . . . 485 e−136 gi|3493013|gb|AAD02964.1| (AF079244) granule-bound starch s . . . 483 e−135 gi|3493039|gb|AAD02977.1| (AF079257) granule-bound starch s . . . 483 e−135 gi|3493015|gb|AAD02965.1| (AF079245) granule-bound starch s . . . 483 e−135 gi|3493031|gb|AAD02973.1| (AF079253) granule-bound starch s . . . 482 e−135 gi|3493001|gb|AAD02958.1| (AF079238) granule-bound starch s . . . 481 e−135 gi|3493017|gb|AAD02966.1| (AF079246) granule-bound starch s . . . 480 e−134 gi|3493009|gb|AAD02962.1| (AF079242) granule-bound starch s . . . 479 e−134 gi|17432494|gb|AAL38185.1| (AY062271) granule-bound starch . . . 479 e−134 gi|13377475|gb|AAK20726.1| (AF318770) granule-bound starch . . . 479 e−134 gi|3493003|gb|AAD02959.1| (AF079239) granule-bound starch s . . . 478 e−133 gi|3493033|gb|AAD02974.1| (AF079254) granule-bound starch s . . . 478 e−133 gi|13774486|gb|AAK38882.1| (AF353520) granule-bound starch . . . 477 e−133 gi|3492999|gb|AAD02957.1| (AF079237) granule-bound starch s . . . 475 e−133 gi|3493101|gb|AAD03008.1| (AF079288) granule-bound starch s . . . 475 e−133 gi|3493109|gb|AAD03012.1| (AF079292) granule-bound starch s . . . 474 e−132 gi|3492997|gb|AAD02956.1| (AF079236) granule-bound starch s . . . 474 e−132 gi|3493027|gb|AAD02971.1| (AF079251) granule-bound starch s . . . 474 e−132 gi|3493029|gb|AAD02972.1| (AF079252) granule-bound starch s . . . 468 e−131 gi|3493107|gb|AAD03011.1| (AF079291) granule-bound starch s . . . 468 e−130 gi|3493117|gb|AAD03016.1| (AF079296) granule-bound starch s . . . 464 e−129 gi|12278453|gb|AAG48967.1| (AY010980) granule-bound starch . . . 462 e−129 gi|12278435|gb|AAG48958.1| (AY010971) granule-bound starch . . . 461 e−129 gi|12278421|gb|AAG48951.1| (AY010964) granule-bound starch . . . 461 e−129 gi|12278479|gb|AAG48980.1| (AY010993) granule-bound starch . . . 461 e−129 gi|12278423|gb|AAG48952.1| (AY010965) granule-bound starch . . . 461 e−128 gi|12278419|gb|AAG48950.1| (AY010963) granule-bound starch . . . 461 e−128 gi|3493081|gb|AAD02998.1| (AF079278) granule-bound starch s . . . 461 e−128 gi|3493071|gb|AAD02993.1| (AF079273) granule-bound starch s . . . 460 e−128 gi|12278471|gb|AAG48976.1| (AY010989) granule-bound starch . . . 460 e−128 gi|12278485|gb|AAG48983.1| (AY010996) granule-bound starch . . . 460 e−128 gi|3493087|gb|AAD03001.1| (AF079281) granule-bound starch s . . . 460 e−128 gi|12278437|gb|AAG48959.1| (AY010972) granule-bound starch . . . 460 e−128 gi|12278449|gb|AAG48965.1| (AY010978) granule-bound starch . . . 459 e−128 gi|12278495|gb|AAG48988.1| (AY011001) granule-bound starch . . . 459 e−128 gi|12278491|gb|AAG48986.1| (AY010999) granule-bound starch . . . 459 e−128 gi|13774484|gb|AAK38881.1| (AF353519) granule-bound starch . . . 459 e−128 gi|3493083|gb|AAD02999.1| (AF079279) granule-bound starch s . . . 459 e−128 gi|12278473|gb|AAG48977.1| (AY010990) granule-bound starch . . . 459 e−128 gi|12278481|gb|AAG48981.1| (AY010994) granule-bound starch . . . 459 e−128 gi|12278413|gb|AAG48947.1| (AY010960) granule-bound starch . . . 459 e−128 gi|3493075|gb|AAD02995.1| (AF079275) granule-bound starch s . . . 458 e−128 gi|12278429|gb|AAG48955.1| (AY010968) granule-bound starch . . . 458 e−128 gi|12278477|gb|AAG48979.1| (AY010992) granule-bound starch . . . 458 e−128 gi|12278463|gb|AAG48972.1| (AY010985) granule-bound starch . . . 458 e−128 gi|12278427|gb|AAG48954.1| (AY010967) granule-bound starch . . . 458 e−128 gi|12278469|gb|AAG48975.1| (AY010988) granule-bound starch . . . 458 e−128 gi|12278411|gb|AAG48946.1| (AY010959) granule-bound starch . . . 458 e−128 gi|13194734|gb|AAK15529.1| (AF331953) granule-bound starch . . . 457 e−127 gi|12278493|gb|AAG48987.1| (AY011000) granule-bound starch . . . 457 e−127 gi|12278431|gb|AAG48956.1| (AY010969) granule-bound starch . . . 457 e−127 gi|12278433|gb|AAG48957.1| (AY010970) granule-bound starch . . . 457 e−127 gi|12278497|gb|AAG48989.1| (AY011002) granule-bound starch . . . 457 e−127 gi|12278425|gb|AAG48953.1| (AY010966) granule-bound starch . . . 457 e−127 gi|12278443|gb|AAG48962.1| (AY010975) granule-bound starch . . . 456 e−127 gi|12278507|gb|AAG48994.1| (AY011007) granule-bound starch . . . 456 e−127 gi|13774480|gb|AAK38879.1| (AF353517) granule-bound starch . . . 456 e−127 gi|12278489|gb|AAG48985.1| (AY010998) granule-bound starch . . . 456 e−127 gi|3493095|gb|AAD03005.1| (AF079285) granule-bound starch s . . . 456 e−127 gi|12278457|gb|AAG48969.1| (AY010982) granule-bound starch . . . 455 e−127 gi|12278451|gb|AAG48966.1| (AY010979) granule-bound starch . . . 455 e−127 gi|3493093|gb|AAD03004.1| (AF079284) granule-bound starch s . . . 455 e−127 gi|3493085|gb|AAD03000.1| (AF079280) granule-bound starch s . . . 455 e−127 gi|3493091|gb|AAD03003.1| (AF079283) granule-bound starch s . . . 455 e−127 gi|13774482|gb|AAK38880.1| (AF353518) granule-bound starch . . . 455 e−127 gi|3493097|gb|AAD03006.1| (AF079286) granule-bound starch s . . . 454 e−127 gi|12278514|gb|AAG48997.1| (AY011011) granule-bound starch . . . 454 e−126 gi|3493111|gb|AAD03013.1| (AF079293) granule-bound starch s . . . 454 e−126 gi|3493051|gb|AAD02983.1| (AF079263) granule-bound starch s . . . 454 e−126 gi|3493073|gb|AAD02994.1| (AF079274) granule-bound starch s . . . 454 e−126 gi|3493113|gb|AAD03014.1| (AF079294) granule-bound starch s . . . 454 e−126 gi|12278509|gb|AAG48995.1| (AY011008) granule-bound starch . . . 454 e−126 gi|3493089|gb|AAD03002.1| (AF079282) granule-bound starch s . . . 454 e−126 gi|12278503|gb|AAG48992.1| (AY011005) granule-bound starch . . . 454 e−126 gi|3493115|gb|AAD03015.1| (AF079295) granule-bound starch s . . . 454 e−126 gi|12278487|gb|AAG48984.1| (AY010997) granule-bound starch . . . 454 e−126 gi|3493119|gb|AAD03017.1| (AF079297) granule-bound starch s . . . 454 e−126 gi|3493077|gb|AAD02996.1| (AF079276) granule-bound starch s . . . 454 e−126 gi|3493103|gb|AAD03009.1| (AF079289) granule-bound starch s . . . 453 e−126 gi|3493099|gb|AAD03007.1| (AF079287) granule-bound starch s . . . 453 e−126 gi|3493079|gb|AAD02997.1| (AF079277) granule-bound starch s . . . 453 e−126 gi|12278417|gb|AAG48949.1| (AY010962) granule-bound starch . . . 452 e−126 gi|3493065|gb|AAD02990.1| (AF079270) granule-bound starch s . . . 452 e−126 gi|3493067|gb|AAD02991.1| (AF079271) granule-bound starch s . . . 452 e−126 gi|12278511|gb|AAG48996.1| (AY011009) granule-bound starch . . . 452 e−126 gi|12278505|gb|AAG48993.1| (AY011006) granule-bound starch . . . 452 e−126 gi|3493049|gb|AAD02982.1| (AF079262) granule-bound starch s . . . 452 e−126 gi|12278501|gb|AAG48991.1| (AY011004) granule-bound starch . . . 451 e−126 gi|12278475|gb|AAG48978.1| (AY010991) granule-bound starch . . . 451 e−125 gi|12278499|gb|AAG48990.1| (AY011003) granule-bound starch . . . 451 e−125 gi|3493055|gb|AAD02985.1| (AF079265) granule-bound starch s . . . 450 e−125 gi|12278415|gb|AAG48948.1| (AY010961) granule-bound starch . . . 449 e−125 gi|3493069|gb|AAD02992.1| (AF079272) granule-bound starch s . . . 448 e−125 gi|13774488|gb|AAK38883.1| (AF353521) granule-bound starch . . . 448 e−125 gi|3493059|gb|AAD02987.1| (AF079267) granule-bound starch s . . . 447 e−124 gi|3493057|gb|AAD02986.1| (AF079266) granule-bound starch s . . . 446 e−124 gi|3493053|gb|AAD02984.1| (AF079264) granule-bound starch s . . . 445 e−124 gi|12278516|gb|AAG48998.1| (AY011012) granule-bound starch . . . 444 e−123 gi|3493105|gb|AAD03010.1| (AF079290) granule-bound starch s . . . 443 e−123 gi|3493121|gb|AAD03018.1| (AF079298) granule-bound starch s . . . 440 e−122 gi|3493063|gb|AAD02989.1| (AF079269) granule-bound starch s . . . 440 e−122 gi|3493061|gb|AAD02988.1| (AF079268) granule-bound starch s . . . 419 e−116 gi|17940636|gb|AAL49705.1| (AF445166) granule-bound starch . . . 405 e−112 gi|17940634|gb|AAL49704.1| (AF445165) granule-bound starch . . . 404 e−111 gi|17940622|gb|AAL49698.1| (AF445159) granule-bound starch . . . 404 e−111 gi|13375389|gb|AAK20309.1| (AF329738) granule bound starch . . . 404 e−111 gi|17940642|gb|AAL49707.1| (AF445170) granule-bound starch . . . 404 e−111 gi|17940630|gb|AAL49702.1| (AF445163) granule-bound starch . . . 404 e−111 gi|17940626|gb|AAL49700.1| (AF445161) granule-bound starch . . . 403 e−111 gi|17940659|gb|AAL49715.1| (AF445179) granule-bound starch . . . 403 e−111 gi|17940644|gb|AAL49708.1| (AF445171) granule-bound starch . . . 403 e−111 gi|17940651|gb|AAL49711.1| (AF445175) granule-bound starch . . . 402 e−111 gi|13375385|gb|AAK20307.1| (AF329736) granule bound starch . . . 402 e−111 gi|17940677|gb|AAL49723.1| (AF445189) granule-bound starch . . . 402 e−111 gi|13375387|gb|AAK20308.1| (AF329737) granule bound starch . . . 402 e−111 gi|17940655|gb|AAL49713.1| (AF445177) granule-bound starch . . . 402 e−111 gi|17940667|gb|AAL49719.1| (AF445183) granule-bound starch . . . 402 e−111 gi|13375399|gb|AAK20314.1| (AF329743) granule bound starch . . . 402 e−111 gi|17940628|gb|AAL49701.1| (AF445162) granule-bound starch . . . 401 e−111 gi|17940639|gb|AAL49706.1| (AF445168) granule-bound starch . . . 401 e−110 gi|17940679|gb|AAL49724.1| (AF445190) granule-bound starch . . . 401 e−110 gi|13375381|gb|AAK20305.1| (AF329734) granule bound starch . . . 400 e−110 gi|17940675|gb|AAL49722.1| (AF445188) granule-bound starch . . . 400 e−110 gi|17940624|gb|AAL49699.1| (AF445160) granule-bound starch . . . 400 e−110 gi|17940648|gb|AAL49710.1| (AF445173) granule-bound starch . . . 400 e−110 gi|17940620|gb|AAL49697.1| (AF445158) granule-bound starch . . . 400 e−110 gi|17940672|gb|AAL49721.1| (AF445186) granule-bound starch . . . 400 e−110 gi|17940653|gb|AAL49712.1| (AF445176) granule-bound starch . . . 399 e−110 gi|17940632|gb|AAL49703.1| (AF445164) granule-bound starch . . . 399 e−110 gi|17940661|gb|AAL49716.1| (AF445180) granule-bound starch . . . 398 e−110 gi|15983795|gb|AAL10494.1| (AY056803) At1g32900/F9L11_8 [Ar . . . 386 e−106 gi|553108|gb|AAA33918.1| (M55039) UDP-glucose starch glycos . . . 379 e−104 gi|13375405|gb|AAK20317.1| (AF329746) granule-bound starch . . . 378 e−103 gi|8778105|gb|AAF79205.1|AF267643_1 (AF267643) starch synth . . . 377 e−103 gi|6116748|dbj|BAA85761.1| (AB028026) granule-bound starch . . . 377 e−103 gi|1136128|gb|AAA84384.1| (U41446) starch synthase [Sorghum . . . 355 7e−97  gi|7433860|pir||T07802 ADPglucose - starch glucosyltransfera . . . 329 5e−89  gi|7433861|pir||T07804 ADPglucose - starch glucosyltransfera . . . 328 1e−88  gi|2829792|sp|P93568|UGS2_SOLTU Soluble glycogen [starch] s . . . 320 4e−86  gi|2833384|sp|Q43093|UGS3_PEA Glycogen [starch] synthase, c . . . 314 2e−84  gi|2129898|pir||S61505 UDPglucose - starch glucosyltransfera . . . 314 2e−84  gi|7489695|pir||T06798 probable starch synthase (EC 2.4.1. - . . . 313 2e−84  gi|8708896|gb|AAC17970.2| (AF026421) soluble starch synthas . . . 312 5e−84  gi|9369336|emb|CAB99210.1| (AJ292522) starch synthase I-2 [. . . 311 2e−83  gi|6103327|gb|AAF03557.1| (AF091802) starch synthase I [Aeg . . . 311 2e−83  gi|15237934|ref|NP_197818.1| (NM_122336) soluble starch syn . . . 310 2e−83  gi|5880466|gb|AAD54661.1| (AF091803) starch synthase I [Tri . . . 310 2e−83  gi|9369334|emb|CAB99209.1| (AJ292521) starch synthase I-1 [. . . 310 3e−83  gi|7188796|gb|AAF37876.1|AF234163_1 (AF234163) starch synth . . . 310 4e−83  gi|15232051|ref|NP_186767.1| (NM_110984) putative glycogen . . . 309 6e−83  gi|6690399|gb|AAF24126.1|AF121673_1 (AF121673) soluble star . . . 308 1e−82  gi|7489710|pir||T01208 ADPglucose - starch glucosyltransfera . . . 308 1e−82  gi|3192881|gb|AAC19119.1| (AF068834) starch synthase [Ipomo . . . 307 3e−82  gi|16265834|gb|AAL16661.1|AF419099_1 (AF419099) putative so . . . 304 2e−81  gi|2833387|sp|Q43654|UGS2_WHEAT Soluble glycogen [starch] s . . . 302 5e−81  gi|7489712|pir||T01414 ADPglucose--starch glucosyltransfera . . . 300 2e−80  gi|2833377|sp|Q40739|UGS2_ORYSA Soluble glycogen [starch] s . . . 300 3e−80  gi|1549232|dbj|BAA07396.1| (D38221) SSS1 [Oryza sativa] >gi . . . 300 3e−80  gi|12019656|gb|AAD45815.2| (AF168786) soluble starch syntha . . . 300 3e−80 

[0384] SSI Amino acid sequence of maize Soluble Starch Synthase I (SSI) Accession: AF036891            NID: g2828011            Mol. wt. (calc) = 67843    Residues = 622 1 M A T P S A V G A A C L L L A R A A W P A A V G D R A R P R SEQ. ID. No. 267 31 R L Q R V L R R R C V A E L S R E G P A P R P L P P A L L A 61 P P L V P G F L A P P A E P T G E P A S T P P P V P D A G L 91 G D L G L E P E G I A E G S I D N T V V V A S E Q D S E I V 121 V G K E Q A R A K V T Q S I V F V T G E A S P Y A K S G G L 151 G D V C G S L P V A L A A R G H R V M V V M P R Y L N G T S 181 D K N Y A N A F Y T E K H I R I P C F G G E H E V T F F H E 211 Y R D S V D W V F V D H P S Y H R P G N L Y G D K F G A F G 241 D N Q F R Y T L L C Y A A C E A P L I L E L G G Y I Y G Q N 271 C M F V V N D W H A S L V P V L L A A K Y R P Y G V Y K D S 301 R S I L V I H N L A H Q G V E P A S T Y P D L G L P P E W Y 331 G A L E W V F P E W A R R H A L D K G E A V N F L K G A V V 361 T A D R I V T V S K G Y S W E V T T A E G G Q G L N E L L S 391 S R K S V L N G I V N G I D I N D W N P A T D K C I F C H Y 421 S V D D L S G K A K C K G A L Q K E L G L P I R P D V P L I 451 G F I G R L D Y Q K G I D L I Q L I I P D L M R E D V Q F V 481 M L G S G D P E L E D W M R S T E S I F K D K F R G W V G F 511 S V P V S H R I T A G C D I L L M P S R F E F C G L N Q L Y 541 A M Q Y G T V P V V H A T G G L R D T V E N F N P F G E N G 571 E Q G T G W A F A P L T T E N M F V D I A N C N I Y I Q G T 601 Q V L L G R A N EA R H V K R L H V G P C R

[0385] TABLE XIII Maize soluble starch synthase I (SSI) Alignments with other similar proteins—Transit Peptide SEQ Accession a.a a.a. Id.No. Number # (start)            Sequence            ending # 268 MAIZESSI 1 MATPSAVGAACLLLARAA-----WPAAVGDXXXXXXXXXXXXXXCVAELSREG--XXXXX 53 269  7489712 1 MATPSAVGAACLLLARAA-----WPAAVGDRARPRRLQRVLRRRCVAELSREG--PAPRP 53 270 12019656 1 MATPSAVGAACLVLARAAAGLGLGPGRGGDRARPRRFQRVVRRRCVAELSREGPAPTPRP 60 271  1549232 34                                             CVAELSRDG--GSAQR 47 272  2833377 34                                             CVAELSRDG--GSAHG 47 273  5295947 34                                             CVAELSRDG--GSAQR 47 268 MaizeSSI 54 XXXXXXXXXXXXXXXXXXXEPTGEPASTPPPVP--------------DAGLGDLG--LEP 97 269  7489712 54 LPPALLAPPLVPGFLAPPAEPTGEPASTPPPVP--------------DAGLGDLG--LEP 97 270 12019656 61 LPPALLAPPLVPAFLAPPSEPEGEPASTFPPLP--------------DAGLGDLG--LQP 104 271  1549232 48 PLAPAPLVKQPVL-------PTFLVPTSTPPAPTQSPAPAPTPPPLPDSGVGEIE--PDL 98 272  2833377 48 PLAPAPLVKQPVL-------PTFLVPTSTPPAPTQSPAPAPTPPPLPDSGVGEIE--PDL 98 273  5295947 48 PLAPAPLVKQPVL-------PTFLVPTSTPPAPTQSPAPAPTPPPLPDSGVGEIE--PDL 98 274  9369336 79                    PAQSPAPTQPPLP--------------DAGVGELAPDLLL 104 275  6103327 79                     PAQSPAPTQPPLP--------------DAGVGELAPDLLL 104 276  9369334 79                     PAQSPAPTQPPLP--------------DAGVGELAPDLLL 104 277  5880466 79                     PAQSPAPTQPPLP--------------DAGVGELAPDLLL 104 278  7188796 75                     PAQSPAPTQPPLP--------------DAGVGELAPDLLL 100 279 16265834 281                                                           EP 282 280  2833381 25                                                  GLGQLA--LRS 33 281   297424 31                                                    GFQG--LKP 37 282    82478 31                                                    GFQG--LKP 37 283  2833382 31                                                    GFQG--LKP 37

[0386] TABLE XIV Maize soluble starch synthase I (SSI) “GLASS” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)            Sequence            ending # 284 MaizeSSI 98 EGIAEG-----SID--NTVVVASEQD--SEIVVGKEQA--R-----AKVT---------- 131 285  7489712 98 EGIAEG-----SID--NTVVVASEQD--SEIVVCKEQA--R-----AKVT---------- 131 287 12019656 105 EGIAEG-----SID--ETVVVASEQD--SEIVVGKEQA--R-----AKVT---------- 138 288  1549232 99 EGLTED-----SID--KTIFVASEQE--SEIMDVKEQA--Q-----AKVT---------- 132 289  2833377 99 EGLTED-----SID--KTIFVASEQE--SEIMDVKEQA--Q-----AKVT---------- 132 290  5295947 99 EGLTED-----SID--KTIFVASEQE--SEIMDVKEQA--Q-----AKVT---------- 132 291  9369336 105 EGIAED-----SID--SIIVAASEQD--SEIMDAKDQP--Q-----AKVT---------- 138 292  6103327 105 EGIAED-----SID--SIIVAASEQD--SEIMDANEQP--Q-----AKVT---------- 138 293  9369334 105 EGIAED-----SID--SIIVAASEQD--SEIMDANEQP--Q-----AKVT---------- 138 294  5880466 105 EGIAED-----SID--SIIVAASEQD--SEIMDANEQP--Q-----AKVT---------- 138 295  7188796 101 EGIAED-----SID--TIVVAASEQD--SEIMDANDQP--L-----AKVT---------- 134 296 15237934 131                                 VGIPSG--K-----AEVV---------- 141 297  6690399 54                                 VGIPSG--K-----AEVV---------- 64 298  2829792 102             VE--SHDIVANDRDDLSEDTEEMEET--P-----IKLT---------- 130 299 15232051 268     EK-----YVE--KTPDVASSET--NE--PGKDEE--KPPPLAGANV---------- 300 300  8708896 65                      AEEEE--PPAVEKPPPL--A-----GPNV---------- 84 301 15384987 126                     VSSADD--SENKESGPLA--G-----PNVM---------- 146 302 15028467 183                     VSSADD--SENKESGPLA--G-----PNVM---------- 203 303 16265834 283 DAAEDG-----DDD--DDWADSDASD--SEIDQDDDSGPLA-----GENV---------- 318 304  5441242 68                                  GREKV--L-----EKIECG-------- 79 305 12003285 54               --NNVKVSAKRV--GQVPINKDRC--E-----TS-G---------- 77 306  2833381 34 QAVTHN-----GLRPVNKIDMLQLRT--SAPNLAKMEG--K-----MRVEWQAGTIVCKQ 79 307   297424 38 RSPAGGDATSLSVT--TSARATPKQQ--RSVQRGSRRF--P-----SVVVYATGAG---- 82 308    82478 38 RSPAGGDATSLSVT--TSARATPKQQ--RSVQRGSRRF--P-----SVVVYATGAG---- 82 309  2833385 78                                          -----ATAG---------- 81 310  2833382 38 RSPAGGDATSLSVT--TSARATPKQQ--RSVQRGSRRF--P-----SVVVYATGAG---- 82 284 (maize SSI) 132 --QSIVFVTGEASPYAKSGGLGDVCGSLPVALAARGHRVMVVMPRYLN-GT-SDKNYANA 187 285  7489712 132 --QSIVFVTGEASPYAKSGGLGDVCGSLPVALAARGHRVMVVMPRYLN-GT-SDKNYANA 187 286 12019656 139 --QSIVFVTGEASPYAKSGGLGDVCGSLPVALAARGHRVMVVMPRYLN-GT-SDKNYANA 194 287  1549232 133 --RSVVFVTGEASPYAKSGGLGDVCGSLPIALALRGNRVMVVMPRYMN-GA-LNKNFANA 188 288  2833377 133 --RSVVFVTGEASPYAKSGGLGDVCGSLPIALAIRGHRVMVVMPRYMN-GA-LNKNFANA 188 289  5295947 133 --RSVVFVTGEASPYAKSGGLGDVCGSLPIALALRGHRVMVVMPRYMN-GA-LNKNFANA 188 290  9369336 139 --RSIVFVTGEAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GS-SDKNYAKA 194 291  6103327 139 --RSIVFVTGEAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GS-SDKNYAKA 194 292  9369334 139 --RSIVFVTGEAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GS-SDKNYAKA 194 293  5880466 139 --RSIVFVTGEAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GS-SDKNYAKA 194 294  7188796 135 --RSIVFVTGEAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GT-SDKNYAKA 190 295  2833387 1 --        EAAPYAKSGGLGDVCGSLPIALAARGHRVMVVMPRYLN-GS-SDKNYAKA 48 296 15237934 142 --NNLVFVTSEAAPYSKTGGLGDVCGSLPIALAGRGHRVMVISPRYLN-GTAADKNYARA 198 297  6690399 65 --NNLVFVTSEAAPYSKTGGLGDVCGSLPIALAGRGHRVMVISPRYLN-GTAADKNYARA 121 298  2829792 131 --FNIIFVTAEAAPYSKTGGLGDVCGSLPMALAARGHRVMVVSPRYLNGGP-SDEKYANA 187 299 15232051 301 --MNVILVAAECAPFSKTGGLGDVAGALPKSLARRGHRVMVVVPRY--------AEYAEA 350 311  3192881 140    NVILVCAECAPWSKTGGLGDVAGALPKALARRGHRVMVVVPLY--------GNYAEP 188 310  2833384 262    NIILVSAECAPWSKTCGLGDVAGSLPKALARRGHRVMIVAPHY--------GNYAEA 310 312  2129898 262    NIILVSAECAPWSKTGGLGDVAGSLPKALARRGHRVMIVAPHY--------GNYAEA 310 313  6467503 261    NVILVAAECAPWSKTGGLGDVAGSLPKALAPRGHRVMVVAPRY--------GNYVEP 309 314 14495348 259    NIILVAAECAPWSKTGGLGDVAGALPKALARRGHRVMVVVPMY--------KNYAEP 307 315  7489711 208    NVVVVASECAPFCKTGGLGDVVGALPKALARRGHRVMVVIPRY--------GEYAEA 256 300  8708896 85 --NNVVMVGAECAPWSKTGGLGDVMAALPKALVRRGHRVMVVVPRY--------ENYDNA 134 301 15384987 147 --NVIV-VASECSPFCKTGGLGDVVGALPKALARRGHRVMVVIPRY--------GEYAEA 195 302 15028467 204 --NVIV-VASECSPFCKTGGLGDVVGALPKALARRGHRVMVVIPRY--------GEYAEA 252 316  7489710 242    NVIVVAAECSPWCKTGGLGDVVGALPKALARRGHRVMVVVPRY--------GDYVEA 290 317  2833390 297    NIILVASECAPWSKTGGLGDVAGALPKALARRGHRVMVVAPRYDN-YP-EPQDSG-- 349 318  7489695 1    NVVVVAAECSPWCKTGGLGDVAGALPKALAKRGHRVMVVVPRY--------GDYEEA 49 319  8953573 308    NVVVVAAECSPWCKTGGLGDVAGALPKALAKRGHRVMVVVPRY--------GDYEEA 356 320  8953571 309    NVVVVAAECSPWCKTGGLGDVAGALPKALAKRGHRVMVVVPRY--------GDYEEA 357 321  7529653 309    NVVVVAAECSPWCKTGGLGDVAGALPKALAKRGHRVMVVVPRY--------GDYEEA 357 303 16265834 319 --MNVIVVAAECSPWCKTGGLGDVAGALPKALARRGHRVMVVVPRY--------GDYAEA 368 322  5825480 309    NVVVVAAECSPWCKTGGLGDVAGALPKALAKRGHRVMVVVPRY--------GDYEEA 357 323  2833388 83    NLIFVGAEVGPWSKTGGLGDVLGGLPRAMAARGHRVMTVSPRY--------DQYKDA 131 304  5441242 80 --MNLIFVGAEVAPWSKTGGLGDVLGGLPSALAEHGHRVMTVSPRY--------DQYKDA 129 305 12003285 78 --MTLIFVSAECGPWSKTGGLGDVVGGLPPALAANRHRVMTVSPRY--------DQYKDA 127 324   267196 82    NLIFVGTEVGPWSKTGGLGDVLGGLPPALAARGHRVMTISPRY--------DQYKDA 130 325   228210 82    NLIFVGTEVGPWSKTGGLGDVLGGLPPALAARGHRVMTISPRY--------DQYKDA 130 326   602594 82    NLIFVGTEVGPWSKTGGLGDVLGGLPPALAARGURVMTISPRY--------DQYKDA 130 327 16716335 61     IVMVAAEVAPWSKTGGLGDVTGGLPIELVKRGHRVMTIAPRY--------DQYADA 108 328  6136121 83    NLVFVLAEVGPWSKTGGLGDVVGGLPPAMAGNGHRVMTVSPRY--------DQYKDA 131 329 15223331 85    SVIFIGAEVGPWSKTGGLGDVLGGLPPALAARGHRVMTICPRY--------DQYKDA 133 330 15626365 88    NLIFVGTEVAPWSKTGGLGDVLGGLPPALSANGHRVMTVTPRY--------DQYKDA 136 331  3832512 82    NLVFVGAEVGPWSKTGGLGDVLGGLPPALAGNGHRVMTVSPRY--------DQYKDA 130 332  2833381 80 QGMNLVFVGCEEGPWCKTGGLGDVLGGLPPAIAARGHRVMTVCPRY--------DQYKDA 131 333 15637079 83    NLVFVGCEVGPWCKTGGLGDVLGGLPPALAARGHRVMTVCPRY--------DQYKDA 131 334  2833383 78    SLVFVGAEVGPWSKTGGLGDVLGGLPPVLAGNGHRVMTVSPRY--------DQYKDA 126 307   297424 83 --MNVVFVGAEMAPWSKTGGLGDVLGGLPPAMAANGHRVMVISPRY--------DQYKDA 132 335    82478 83 --MNVVFVGAEMAPWSKTGGLGDVLGGLPPAMAANGHRVMVISPRY--------DQYKDA 132 309  2833385 82 --MNVVFVGAEMAPWSKTGGLGDVLGGLPPAMAANGHRVMVVSPRY--------DQYKDA 131 336  2833382 83 --MNVVFVGAEMAPWSKTGGLGDVLGGLPPAMAANGHRVMVISPRY--------DQYKDA 132 284 (maize SSI) 188 FYTEKHIRIPCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------H-R-P------G-N 230 285  7489712 188 FYTEKHIRIPCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------N-R-P------G-N 230 286 12019656 195 FYTEKHIRIFCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------H-R-P------G-N 237 287  1549232 189 FYTEKHIKIPCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------H-R-P------G-N 231 288  2833377 189 FYTEKHIKIPCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------H-R-P------G-N 231 289  5295947 189 FYTEKHIKIPCFGGEHE-VTFFHEYRDSVDWVFV-DHPSY------H-R-P------G-N 231 290  9369336 195 LYTAKHIKIPCFGGSHE-VTFFHEYRDNVDNVFV-DHPSY------H-R-P------G-S 237 292  6103327 195 LYTAKHIKIPCFGGSHE-VTFFHEYRDNVDWVFV-DHPSY------H-R-P------G-S 237 292  9369334 195 LYTGKHIKIPCFGGSHE-VTFFHEYRDNVDWVFV-DHPSY------H-R-P------G-S 237 293  5880466 195 LYTGKHIKIPCFGGSHE-VTFFHEYRDNVDWVFV-DHPSY------H-R-P------G-S 237 294  7188796 191 LYTGKUIKIPCFGGSHE-VTFFHEYRDNVDWVFV-DHPSY------H-R-P------G-S 233 295  2833387 49 LYTAKHIKIPCFGGSHE-VTFFHEYRDNVDWVFV-DHPSY------H-R-P------G-S 91 296 15237934 199 KDLGIRVTVNCFGGSQE-VSFYHEYRDGVDWVFV-DHKSY------H-R-P------G-N 241 297  6690399 122 KDLGIRVTVNCFGGSQE-VSFYHEHRDGVDWVFV-DHKSY------H-R-P------G-N 164 298  2829792 188 VDLDVRAIVHCFGDAQE-VAFYHEYRAGVDWVFV-DHSSY------C-R-P------G-T 230 299 15232051 351 KDLGVRKRYKVAGQDME-VMYFHAFIDGVDFVFI-DSPEFR-----H-L-S------N-N 394 311  3192881 189 QHTGVRKMFKIDGQDME-VNYFHAYIDNVDFVFI-DSPIFQ-----H-R-G------N-N 232 310  2833384 311 HDIGVRKRYKVAGQDME-VTYFHTYIDGVDIVFI-DSPIF------R-NLE------S-N 354 312  2129898 311 HDIGVRKRYKVAGQDME-VTYFHTYIDGVDIVFI-DSPIF------R-NLE------S-N 354 313  6467503 310 QDTGVRKRYKVDGQDFE-VSYFQAFIDGVDFVFI-DSPMF------R-H-I------G-N 352 314 14495348 308 QQLGEPRRYQVAGQDME-VIYYHAYIDGVDFVFI-DNPIF------H-H-V------E-N 350 315  7489711 257 RDLGVRRRYKVAGQDSE-VTYFHSYIDGVDFVFV-EAPPFR-----H-R-H------N-N 300 300  8708896 135 WETGIRKIYSVFNSNQE-VGYFHAFVDGVDYVFV-DHPTF------HGR-G------K-N 178 301 15384987 196 KDLGVRKRYRVAGQDSE-VSYFHAFIDGVDFVFL-EAPPFR-----H-R-H------N-D 239 302 15028467 253 KDLGVRKRYRVAGQDSE-VSYFHAFIDGVDFVFL-EAPPFR-----H-R-H------N-D 296 316  7489710 291 FDMGIRKYYKAAGQDLE-VNYFHAFIDGVDFVFI-DAPLFR-----H-R-Q------D-D 334 317  2833390 350 --VRKIYKVD--GQDVD-VTYFQALLMDCDFVFIHSHMFR------H-I-G------N-N 389 318  7489695 50 YDVGVRKYYKAAGQDME-VNYFHAYIDGVDFVFI-DAPLFR-----H-R-Q------E-D 93 320  8953573 357 YDVGVRKYYKAAGQDME-VNYFHAYIDGVDFVFI-DAPLFR-----H-R-Q------E-D 400 320  8953571 358 YDVGVRKYYKAAGQDME-VNYFHAYIDGVDFVFI-DAPLFR-----H-R-Q------E-D 401 321  7529653 358 YDVGVRKYYKAAGQDME-VNYFHAYIDGVDFVFI-DAPLFR-----H-R-Q------E-D 401 303 16265834 369 QDVGIRKYYKAAGQDLE-VKYFHAFIDGVDFVFI-DAPLFR-----H-R-Q------D-D 412 322  5825480 358 YDVGVRKYYKAAGQDME-VNYFHAYIDGVDFVFI-DAPLFR-----H-R-Q------E-D 401 323  2833388 132 WDTSVSVEIKIGDRIET-VRFFHSYKRGVDRVFV-DHPMF------L-E-KVWGKTGS-K 180 304  5441242 130 WDTNVTVEVKVADRIET-VRFFHCYKQGVDRVFV-DHPCF------L-E-KVWGKTGS-K 178 305 12003285 128 WDTSVVVEIQVGDKVET-VGFFHCYKRGVDRVFV-DHPLFLEKVWGK-T-K------S-K 176 324   267196 131 WDTSVAVEVKVGDSIEI-VRFFHCYKRGVDRVFV-DHPMF------L-E-KVWGKTGS-K 179 325   228210 131 WDTSVAVEVKVGDSIEI-VRFFHCYKRGVDRVFV-DHPMF------L-E-KVWGKTGS-K 179 326   602594 131 WDTSVAVEVKVGDSIEI-VRFFHCYKRGVDRVFV-DHPMF------L-E-KVWGKTGS-K 179 327 16716335 109 WDTSVVVDIM---GE-K-VRYFHSIKKGVHRVWI-DHPWFLAKVWGK-T-G------S-K 153 328  6136121 132 WDTSVVVEIKVGDSIET-VRFFHCYKRGVDRVFV-DHPIFLEKVWGK-T-K------S-K 180 329 15223331 134 WDTCVVVQIKVGDKVEN-VRFFHCYKRGVDRVFV-DHPIFLAKVVGK-T-G------S-K 182 330 15626365 137 WDTNVTIEVKVGDRTEK-VRFFHCFKRGVDRVFV-DHPIF------L-E-KVWGKTGT-K 185 331  3832512 131 WDTGVSVEIKVGDRFET-VRFFHCYKRGVDRVFV-DHPLFLEKVWGK-T-E------S-K 179 332  2833381 132 WETCVVVE-PQVGDRIEPVRFFHSYKRGVDRVFV-DHPMFLEKVW-G-K-T------G-S 179 333 15637079 132 WDTCVVVELQVGDRIEP-VRFFHSYKRGVDRVFV-DHPMFLEKVE-G-K-T------G-S 179 334  2833383 127 WDTNVLVEVKVGDKIET-VRFFHCYKRGVDRVFV-DHPLFLERVWGK-T-G------S-K 175 307   297424 133 WDTSVVAEIKVADRYER-VRFFHCYKRGVDRVFI-DHPSFLEKVW-G-K-T------GEK 181 335    82478 133 WDTSVVAEVKVADRYER-VRFFHCYKRGVDRVFI-DHPSFLEKVW-G-K-T------GEK 181 309  2833385 132 WDTSVVSEIKMGDGYET-VRFFHCYKRGVDRVFI-DHPLFLERVWGK-T-E------E-K 180 310  2833382 133 WDTSVVAEIKVADRYER-VRFFRCYKRGVDRVFI-DHPSFLEKVW-G-K-T------GEK 181 284 (Maize SSI) 231 -LYGDKFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 271 285  7489712 231 -LYGDKFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 271 286 12019656 238 -LYGDKFG-A-FGDNQFRYTLLCYAACEAPLVLEL--GG--Y-----I-----YG-Q-NC 278 287  1549232 232 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-KC 272 288  2833377 232 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-KC 272 289  5295947 232 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-KC 272 290  9369336 238 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 278 291  6103327 238 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 278 292  9369334 238 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 278 293  5880466 238 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 278 294  7188796 234 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-SC 274 295  2833387 92 -LYGDNFG-A-FGDNQFRYTLLCYAACEAPLILEL--GG--Y-----I-----YG-Q-NC 132 296 15237934 242 -PYGDSKG-A-FGDNQFRFTLLCHAACEAPLVLPL--GG--F-----T-----YG-E-KS 282 297  6690399 165 -PYGDSKG-A-FGDNQFRFTLLCHAACEAPLVLPL--GG--F-----T-----YG-E-KS 205 298  2829792 231 -PYGDIYG-A-FGDNQFRFTLLSHAACEAPLVLPL--GG--F-----T-----YG-E-KC 271 299 15232051 395 -IYG---G-N-RLDILKRMVLFCKAAVEVPWYVPC--GG--V-----C-----YG-DGNL 433 311  3192881 233 -IYG---G-N-RVDILKRMDLFCKAAIVVPWHVPC--GG--I-----C-----YG-DGNL 271 310  2833384 355 -IYG---G-N-RLDILRRMVLFCKAAVEVPWHVPC--GG--I-----C-----YG-DGNL 393 312  2129898 355 -IYG---G-N-RLDILRRMVLFCKAAVEVPWHVPC--GG--I-----C-----YG-DGNL 393 313  6467503 353 DIYG---G-N-RMDILKRMVLFCKAAVEVPWHVPC--GG--V-----C-----YG-DGNL 392 314 14495348 351 DIYG---G-D-RTDILKRMVLLCKAAIEVPWYVPC--GG--Y-----C-----YG-DGNL 390 315  7489711 301 -IYG---G-E-RLDILKRMILFCKAAVEVPWYAPC--GG--T-----V-----YG-DGNL 339 300  8708896 179 -IYG---G-E-RQEILFRCALLCKAALEAVWHVPC--GG--I-----T-----YGDD-NL 217 301 15384987 240 -IYG---G-E-RFDVLKRMILFCKAAVEVPWFAPC--GG--S-----I-----YG-DGNL 278 302 15028467 297 -IYG---G-E-RFDVLKRMILFCKAAVEVPWFAPC--GG--S-----I-----YG-DGNL 335 316  7489710 335 -IYG---G-S-RQEIMKRMILFCKVAVEVPWHVPC--GG--V-----C-----YG-DGNL 373 317  2833390 390 -IYG---G-N-RVDILKRMVLFCKAAIEVPWHVPC--GG--V-----C-----YG-DGNL 428 318  7489695 94 -IYG---G-S-RQEIMKRMVLFCIAVEVPVWHVPC--GG--V-----P-----YG-DGNL 132 319  8953573 401 -IYG---G-S-RQEIMKPMILFCKAAVEVPWHVPC--GG--V-----P-----YG-DGNL 439 320  8953571 402 -IYG---G-S-RQEIMKRMILFCKAAVEVPWHVPC--GG--V-----P-----YG-DGNL 440 321  7529653 402 -IYG---G-S-RQEIMKRMILFCKAAVEVPWHVPC--GG--V-----P-----YG-DGNL 440 303 16265834 413 -IYG---G-N-RQEIMKRMILFCKAAVEVPWHVPC--GG--V-----P-----YG-DGNL 451 322  5825480 402 -IYG---G-S-RQEIMKPMILFCKAAVEVPWHVPC--GG--V-----F-----YG-DGNL 440 323  2833388 181 -IYGPFAG-LDYQDNQLRFSLLCLAALEAPRVLNL--NS--S-----KNFSGPYG-E-EV 227 304  5441242 179 -LYGPSAG-VDYEDNQLRYSLLCQAALEAPRVLNL--NSNKY-----FSGP--YG-E-DV 225 305 12003285 177 -VYGPSAG-VDYEDNQLRFSLLSLAALEAFRVLNL--TSNKY-----FSGP--YG-E-DV 223 324   267196 180 -IYGPKAG-LDYLDNELRFSLLCQAALEAPKVLNLNSSN--Y-----FSGP--YG-E-DV 226 325   228210 180 -IYGPKAG-LDYLDNELRFSLLCQAALEAPKVLNLNSSN--Y-----FSGP--YG-E-DV 226 326   602594 180 -IYGPKAG-LDYLDNELRFSLLCQAALEAPKVLNLNSSN--Y-----FSGP--YG-E-DV 226 327 16716335 154 -LYGPRSG-ADYLDNHKRFALFCKAAIEAARVLPF--GP---------------G-E-DC 192 328  6136121 181 -IYGPNAG-TDYQDNQLRFSLLCQAALEAPRVLNLTSSK--Y-----FSGP--YG-E-DV 227 329 15223331 183 -IYGPITG-VDYNDNQLRFSLLCQAALEAPQVLNL--NSSKY-----FSGF--YG-E-DV 229 330 15626365 186 -LYGPAAGDD-YQDNQLRFSIFCQAALEAARVLNL--KSNKY-----FSGP--YG-E-DV 232 331  3832512 180 -LYGPKTG-VDYKDNQLRFSLLCQAALEAPRVLNL--NS--N-----KHFSGPYG-E-DV 226 332  2833381 180 MLYGPKAG-KDYKDNQLRFSLLCQAALEAPRVLNLNSSN--Y-----FSGP--YG-E-DV 227 333 15637079 180 MLYGPKAG-KDYKDNQLRFSLLCQAALEAPRVLNLNSSN--Y-----FSGP--YG-E-DV 227 334  2833383 176 -LYGPKTG-IDYRDNQLRFSLLCQAALEAPRVLNL--NSSKY-----FSGP--YG-E-DV 222 307   297424 182 -IYGPDTG-VDYKDNQMRFSLLCQAALEAPRILNL--NN--NPYFKGT-----YG-E-DV 228 335    82478 182 -IYGPDTG-VDYKDNQMRFSLLCQAALEAPRILNL--NN--NPYFKGT-----YG-E-DV 228 309  2833385 181 -KYGPDAG-TDYKDNQLRFSLLCQAALEAPRILSL--NNNPY-----FSGP--YG-E-DV 227 310  2833382 182 -IYGPDTG-VDYKDNQMRFSLLCQAALEAPRILNL--NN--NPYFKGT-----YG-E-DV 228 284 (maize 881) 272 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 331 285  7489712 272 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEQYG 331 286 12019656 279 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEQYG 338 287  1549232 273 MFVVNDWHASLVPVLLAAKYRPYGVYPDSRSILVIHNLAHQGVEPASTYPDLGLPPEQYG 332 288  2833377 273 MFVVNDWHASLVPVLLAAKYRPYGVYRDSRSILVIHNLAHQGVEPASTYPDLGLPPEQYG 332 289  5295947 273 MFVVNDWHASLVPVLLAAKYRPYGVYRDSRSILVIHNLAHQGVEPASTYPDLGLPPEQYG 332 290  9369336 279 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 338 291  6103327 279 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 338 292  9369334 279 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 338 293  5880466 279 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 338 294  7188796 275 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 334 295  2833387 133 MFVVNDWHASLVPVLLAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYG 192 296 15237934 283 LFLVNDWHAGLVPILLAAKYRPYGVYKDARSILIIHNLAHQGVEPAATYTNLGLPSEWYG 342 297  6690399 206 LFLVNDWHAGLVPILLAAKYRPYGVYKDARSILIIHNLAHQGVEPAATYTNLGLPSEWYG 265 298  2829792 272 LFLANDWHAALVPLLLAAKYRPYGVYKDARSIVAIHNIAHQGVEPAVTYNNLGLPPQWYG 331 299 15232051 434 AFIANDWHTALLPVYLKAYYPRDHGIMDYTRSVLVIHNIAHQGRGPVDFSYVDLPSHYLD 493 311  3192881 272 VFIANDWHTALLPVYLKAYFRDNGVMKFTRSVLVIHNIAHQGRGPMDDFSIVDLPAQYAD 331 310  2833384 394 VFIABDWHTALLPVYLKAYYRDHGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLD 453 312  2129898 394 VFIABDWHTALLPVYLKAYYRDHGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLD 453 313  6467503 393 AFIANDWHTALLPVYLKAYYRDNGLMQYTRSVLVIHNIAHQGRGPSGDFSYVGLPEHYI- 451 314 14495348 391 VFLANDWHTALLPVYLKAYYHDNGFMIYARSVLVIHNIAHQGRGPLDDFSYLDLPVDYMD 450 315  7489711 340 VFIANDWHTALLPVYLKAYYRDNGLMQYARSVLVIHNIAHQGRGPVDDFVNFDLPEHYID 399 300  8708896 218 CFIANDWHTALLPVYLQAHYRDYGEMTYARCAFVIHNMAHQGRGPFVESEHLELNEE--- 274 301 15384987 279 VFIANDWHTALLPVYLKAYYRDNGLMQYTRSVLVIHNIAHQGRGPVDDFATMDLPEHYID 338 302 15028467 336 VFIANDWHTALLPVCLKAYYRDNGLMQYTRSVLVIHNIAHQGRGPVDDFATMDLPEHYID 395 316  7489710 374 VFIANDWHTALLPVYLKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQ 433 317  2833390 429 VFIANDWHTALLPAYLKAYYRDNGIMNYTRSVLVIHNIAHQGRGPLEDFSYVDLPPHYMD 488 318  7489695 133 VFIANDWHTALLPVYLKAYYRDHGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYL- 191 319  8953573 440 VFIANDWHTALLPVYLKAYYPHGIJMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYL- 498 320  8953571 441 VFIANDWHTALLPVYLKAYYRDHGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYL- 499 321  7529653 441 VFIANDWNTALLPVYLKAYYRDHGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYL- 499 303  1626583 4452 VFLANDWHTALLPVYLKAYYRDNGMMQYTRSVILVIHNAYQGRGPVDEFPYMELPEHYLD 511 322  5825480 441 VFIANDWHTALLPVYLKAYYRDHGLMQYTRSIMVIHINAHQGRGPVDEFPFTELPEHYL- 499 323  2833388 228 AFIANDWHTALLPCYLKAIYQPMGIYKHAKVAFCIHNIAYQGRFAFSDFPRLNLPDKEFS 287 304  5441242 226 IFVANDWHTALLPCYLKSMYQTRGVYRNTKVAFCIHNISYQGRHPFEDFPLLNLPNEYRS 285 305 12003285 224 VFVANDWHTAVLPCYLKTIYQPKGIYTNAKVVLCIHNIAYQGRFAFSDFYKLNLPDQLKS 283 324   267196 227 LFIANDWHTALIFCYLKSMYQSRGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRG 286 325   228210 227 LFIANDWHTALIFCYLKSMYQSRGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRG 286 326   602594 227 LFIANDWHTALIFCYLKSMYQSRGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRG 286 327 16716335 193 VFVANDWHSALVPVLLKDEYQPKGQFTKAKSVLAIHNIAFQGRNWEEAFKDTKLPQAAFD 252 328  6136121 228 VFVANDWHTALLPCYLKSMYQSKGMYLHAKVAFCIHNIAYQGRFGSSDFCLLNLPDQFKS 287 329 15223331 230 VFVANDWNTALLPCYLKSMYQSRGVYMNAKVVFCIHNIAYQGRFAFDDYSLLNLPISFKS 289 330 15626365 233 IFVANDWHTALISCYMKSMYQSIGIFRNAKVVFCIHNIAYQGRFAFTDYSLLNLPDQFKS 292 331  3832512 227 VFVANDWHTALLPCYLKSLYKSKGIYKSAKVAFCIHNIAYQGRHAFSDLSLLNLPNEFRS 286 332  2833381 228 VFVANDWHTALLPCYLKTMYQSRGIYMNAKVAFCIHNIAYQGRFAFSDFSLLNLPDEYKG 287 333 15637079 228 VFVANDWHTALLPCYLKTMYQSRGIYMNAKVAFCIHNIAYQGRFAFSDFSLLNLPDEYKG 287 332  2833383 223 IFVANDWHSALIPCYLKSMYKSRGLYKNAKVAFCIHNIAYQGRNAFSDFSLLNLPDEFRS 282 307   297424 229 VFVCNDWHTGPLASYLKNNYQPNGIYFNAKVAFCIHNISYQGRFAFEDYPELNLSERFRS 288 335    82478 229 VFVCNDWHTGPLASYLKNNYQPNGIYPNAKVAFCIHNISYQGRFAFEDYPELNLSERFRS 288 309  2833385 228 VFVCNDWHTGPLSCYLKSNYQSNGIYKDAKTAFCIHNISYQGRFAFSDFPELNLPERFKS 287 310  2833382 229 VFVCNDWHTGPLASYLKSNYQPNGIYRNAKVAFCIHNISYQGRFAFEDYPELNLSERFRS 288

[0387] TABLE XV Maize soluble starch synthase I (SSI) “LINKR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)            Sequence            ending # 336 MaizeSSI 332 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSKGYSWE 375 337  7489712 332 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSKGYSWE 375 338 12019656 339 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSKGYSWE 382 339  1549232 333 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 376 340  2833377 333 ALEW------VFPEWARRRALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 376 341  5295947 333 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 376 342  9369336 339 ALEW------VFPEWARREALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 382 343  6103327 339 ALEW------VFPEWARRRALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 382 344  9369334 339 ALEW------VFPEWARPRALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 382 345  5880466 339 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 382 346  7188796 335 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 378 347  2833387 193 ALEW------VFPEWARRHALD---KG-------EAVNFLKGAVVTADRIVTVSQGYSWE 236 348 15237934 343 AVGW------VFPTWARTHALD---TG-------EAVNVLKGAIVTSDRIITVSQGYAWE 386 349  6690399 266 AVGW------VFPTWARTHALD---TG-------EAVNVLKGAIVTSDRIITVSQGYAWE 309 350  2829792 332 AVEW------IFPTWAPAHALD---TG-------ETVNVLKGAIAVADRILTVSQGYSWE 375 351 15232051 494 SFKL------YDPV-----------GG-------EHFNIFAAGLKAADRVLTVSHGYSWE 529 352  3192881 332 LFKL------YDPV-----------GG-------DHFNIFAAGLKTADRVVTVSHGYAWE 367 353  2833384 454 LFKM------YDPV-----------GG-------EHFNIFAAGLKTADRIVTVSHGYAWE 489 354  2129898 454 LFKM------YDPV-----------GG-------EHFNIFAAGLKTADRIVTVSHGYAWE 489 355  6467503 452 -------------DLFKLHDFI---GG-------DHFNIFAPGLKVADRVVTVSHGYAWE 488 356 14495348 451 LFKL------YDPF-----------GG-------DHLNIFAAGIKAADRLLTVSHGYAWE 486 357  7489711 400 HF--------------KLYDNI---GG-------DHSNVFAAGLKTADRVVTVSNGYNWE 435 358  8708896 275 -----------YRERFRLYDPI---GG-------EHMNVMKAGLECAHRLVAVSKCYAWE 313 359 15384987 339 HFRL------YDPV-----------GG-------EHSNVFAAGLKMADRAVTVSHGYLWE 374 360 15028467 396 HFRL------YDPV-----------GG-------EHSNVFAAGLKMADPAVTVSHGYLWE 431 361  7489710 434 HFRL------YDPV-----------GG-------EHANIFAAGLKMADRVVTVSRGYLWE 469 362  2833390 489 PFKL------YDPV-----------GG-------EHFNIFAAGLKTADRVVTVSHGYSWE 524 363  7489695 192 -------------EHFRLYDPV---GG-------EHANYFAAGLKMADQVVVVSPGYLWE 228 364  8953573 499 -------------EHFRLYDPV---GG-------EHANYFAAGLKMADQVVVVSPGYLWE 535 365  8953571 500 -------------EHFRLYDFV---GG-------EHANYFAAGLKMADQVVVVSPGYLWE 536 366  7529653 500 -------------EHFRLYDPV---GG-------EHANYFAAGLKMADQVVVTSPGYLWE 536 367 16265834 512 HFKLY-------YDPV---------GG-------EHANIFGAGLKMADRVVVTSPGYLWE 547 368  5825480 500 -------------EHFRLYDPV---GG-------EHANYFAAGLKMADQVVVVSPGYLWE 536 369  2833388 288 SFDF------I----DGYEKPV---KG-------RKINWMKAGILESDRVLTVSPYYAQE 327 370  5441242 286 AFD--------FTDGHLKPV-----RG-------RKINWMKAAILESDLVLTVSPYYAKE 325 371 12003285 284 SFD--------FMDGYEKPV-----KG-------RKINWMKAGIIESDRVLTVSPYYAKE 323 372   267196 287 SFDF------I----DGYEKPV---KG-------RKINWMKAGILESHRVVTVSPYYAQE 326 373   228210 287 SFDF------I----DGYEKPV---KG-------RKINWMKAGILESHRVVTVSFYYAQE 326 374   602594 287 SFDF------I----DGYEKPV---KG-------RKINWMKAGILESHRVVTVSPYYAQE 326 375 16716335 253 KLAFSDGYAKVYTEATPMEEDE---KPPLTGKTYKKINWLKGGIIAADKLVTVSPNYATE 309 376  6136121 288 SFDF-------FDGYEKP---V---KG-------RKINWMKAGILESDRVVTVSPYYAQE 327 377 15223331 290 SFD--------FMDGYEKPV-----KG-------RKINWMKAAILEAHRVLTVSPYYAQE 329 378 15626365 293 SFDFLDGH--VKPIVGRK------------------INWMKAGIIESHRVLTVSPYYAQE 332 379  3832512 287 SFDF------I-------DGYDKPVKG-------RKINWNKAGVLESDRVFTVSPYYAKE 326 380  2833381 288 SFDF------I-------DGYDKPVKG-------RKINWMKAGIREADRVFTVSPNYAYE 327 381 15637079 288 SFDF------I-------DGYDKFVKG-------RKINWMKAGIREALRVFTVSPNYAKE 327 382  2833383 283 SFDF------I----DGYNKPC---EG-------RKINWMKAGILESDQVFTVSPHYAKE 322 383   297424 289 SFDF------I-------DGYDTPVEG-------RKINWMKAGILEADRVLTVSPYYAEE 328 384    82478 289 SFDF------I-------DGYDTPVEG-------RKINWMKAGILEADRVLTVSPYYAEE 328 385  2833385 288 SFDF------I----DGYEKPV---EG-------RKINWMKAGILEADRVLTVSPYYAEE 327 386  2833382 289 SFDF------I-------DGYDTPVEG-------RKINWNKAGILEADRVLTVSPYYAEE 328

[0388] TABLE XVI Maize soluble starch synthase I (SSI) “GLYTR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                  Sequence                  end # 387 NaizeSSI 376 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPATDKCIP-----CHY-SVDD- 424 388  7489712 376 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPATDKCIP-----CHY-SVDD- 424 389 12019656 383 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPATDKCIP-----CHY-SVDD- 431 390  1549232 377 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPSTDKFLP-----YHY-SVDD- 425 391  2833377 377 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPSTDKFLP-----YHY-SVDD- 425 392  5295947 377 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPSTDKFLP-----YHY-SVDD- 425 393  9369336 383 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 431 394  6103327 383 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 431 395  9369334 383 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 431 396  5880466 383 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 431 397  7188796 379 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 427 398  2833387 237 -VTT-A-EG-GQGLNELLSSRKSVLNGIVNGIDINDWNPTTDKCLP-----HHY-SVDD- 285 399 15237934 387 -ITT-V-EG-GYGLQDLLSSRKSVINGITNGIDINEWNPSTDEHIP-----FHY-SADD- 435 400  6690399 310 -ITT-V-EG-GYGLQDLLSSRKSVINGITNGINVDEWNPSTDEHIP-----FHY-SADD- 358 401  2829792 376 -ITT-P-EG-GYGLHELLSSRQSVLNGITNGIDVNDWNPSTDEHIP-----SHY-SIND- 424 402 15232051 530 -VKT-L-EG-GWGLHNIINENDWKFRGIVNGIDTQEWNPEFDTYLHSDDY-TNY-SLEN- 582 403  3192881 368 -LKT-S-EG-GWGLNGIRNENEWKLQGIVNGIDIEEWNPQLDVYLKSDGY-ANY-SLDT- 420 404  2833384 490 -LKT-S-EG-GWGLHNIINESDWKFRGIVNGVDTKDWNPQFDAYLTSDGY-TNY-NLKT- 542 405  2129898 490 -LKT-S-EG-GWGLHNIINESDWKFRGIVNGVDTKLWNPQFDAYLTSDGY-TNY-NLKT- 542 406  6467503 489 -LKT-S-EG-GWGLHNIINENHWKLQGIVNGIDAKEWNPQFDIQLTSDGY-TNY-SLET- 541 407 14495348 487 -LKT-A-EG-GWGLHGIINESDWKFQGIVNGIDTTDWNPRCDIHLKSDGY-TNY-SLET- 539 408  7489711 436 -LKT-S-EG-GWGLNDIINQNDWKLQGIVNGIDMSEWNPAVD---------VHL-HSDD- 480 409  8708896 314 -CQT-V-EG-GWGLHEVIIKNNWKLRGIVNGIDYKEWNPICDEFLTTDGY-AHY-DVDT- 366 410 15384987 375 -IKT-M-DG-GWGLHEIINIIDWKLQGIVNGIDMAEWNPEVDEHLQSDGY-ANY-TFET- 427 411 15028467 432 -IKT-M-DG-GWGLHEIINENDWKLQGIVNGIDMAEWNPEVDEHLQSDGY-ANY-TFET- 484 412  7489710 470 -LKT-V-EG-GWGLHDIIRSNDWKINGIVNGIDHQEWNPKVDVHLRSDGY-TNY-SLET- 522 413  2833390 525 -LKT-S-QG-GWGLHQIINENDWKLQGIVNGIDTKEWNPELDNHLPRSDGYMNY-SLDT- 578 414  7489695 229 -LKT-V-EG-GWGLHDIIRQNDWKTRGIVNGIDNMEWNPEVDAHLKSDGY-TNF-SLRT- 281 415  8953573 536 -LKT-V-EG-GWGLHDIIRQNDWKTRGIVNGIDNMEWNPEVDAHLKSDGY-TNF-SLGT- 588 416  8953571 537 -LKT-V-EG-GWGLHDIIRQNDWKTRGIVNGIDNNEWNPEVDVHLKSDGY-TNF-SLST- 589 417  7529653 537 -LKT-V-EG-GWGLHDIIRQNDWKTRGIVNGIDNNEWNPEVDVHLKSDGY-TNF-SLRT- 589 418 16265834 548 -LKT-T-EG-GWGLHDIIRENDWKTRGIVGIDYREWNPEVDVHLQSDGYY-ANY-TVAS- 600 419  5825480 537 -LKT-V-EG-GWGLHDIIRQNDWTRGIVNGIDNMEWNPEVDVHLQSDGYY-TNF-SLGT- 589 420  2833388 328 -VIS-GVER-GVELDNFI--RKTGIAGIINGMDVQEWNPVTDKYID-----IHY-DATTV 376 421  5441242 326 -LVS-G-EDRGVELDNII--RKTGVAGIVNGMDIREWSPKTDKYID-----IHF-DTTS- 373 422 12003285 324 LVSG-P-DK-GVELDNIL--RKCTVTGIVNGMDTQEWNPATDKYID-----NHY-DITTV 372 423   267196 327 -LVS-AVDK-GVELDSVL--RKTCITGIVNGMDTQEWNPATDKYTD-----VKY-DITTV 375 424   228210 327 -LVS-AVDK-GVELDSVL--RKTCITGIVNGMDTQEWNPATDKYTD-----VKY-DITTV 375 425   602594 327 -LVS-AVDK-GVELDSVL--RKTCITGIVNGMDTQEWNPATDKYTD-----VKY-DITTV 375 426 16716335 310 -IAADA-AG-GVELDTVI--RAKGIEGIVNGMDIEEWNPKTDKFLS-----VPY-DQNS- 357 427  6136121 328 LVSG-A-EK-GVELDNVIA--KTSITGIVNGMDTQEWNPATDKHID-----TNY-DITTV 376 428 15223331 330 LISG-V-DR-GVELHKYL--RMKTVSGIINGMDVQEWNPSTDKYID-----IKY-DITT- 377 429 15626365 333 LVSG-P-DK-GVELDNIL--RRVGVTGIVNGMDVQEWNPSTDKYIS-----IKY-DASTV 381 430  3832512 327 -LVS-G-EDRGVELDNII--RSIGITGIVNGMDNREWSPQTDRYID-----VHY-DAST- 374 431  2833381 328 LVSC-V-SK-GVELDNHI--RDCGITGICNGMDTQEWNPATDKYLA-----VKY-DITTV 376 432 15637079 328 LVSC-V-SK-GVELDNHI--RDCGITGICNGMDTQEWNPATDKYLA-----VKY-DITTV 376 433  2833383 323 -LIS-G-EDRGVELDNII--RSTGIIGIVNGMDNREWSPQTDRYID-----VHY-NETT- 370 434   297424 329 -LIS-G-IARGCELDNIM--RLTGITGIVNGMDVSEWDPSKDKYIT-----AKYDATTA- 377 435    82478 329 -LIS-G-IARGCELDNIM--RLTGITGIVNGMDVSEWDPSKDKYIT-----AKYDATTA- 377 436  2833385 328 -LIS-G-IARGCELDNIM--RLTGITGIVNGMDVSEWDPSKDKYIA-----VKY-DVSTA 376 437  2833382 329 -LIS-G-IARGCELDNIM--RLTGITGIVNGMDVSEWDPSKDKYIT-----AKYDATTA- 377 387 Maize SSI 425 L---------S-GKAKCKGALQKELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLM- 473 388  7489712 425 L---------S-GKAKCKGALQKELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLM- 473 389 12019656 432 L---------S-GKAKCKSALQKELGLPIRPEVPLIGFIGRLDYQKGIDLIQLIIPHLM- 480 390  1549232 426 L---------S-GKAKCKAELQKELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLM- 474 391  2833377 426 L---------S-GKAKCKAELQKELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDLM- 474 392  5295947 426 L---------S-GKAKCKAELQKELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDLM- 474 393  9369336 432 L---------S-GKAKCKAELQKELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPELM- 480 394  6103327 432 L---------S-GKAKCKAELQKELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPELM- 480 395  9369334 432 L---------S-GKAKCKAELQKELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPELM- 480 396  5880466 432 L---------S-GKAKCKAELQKELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPELM- 480 397  7188796 428 L---------S-GKAKCKAELQRELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPDLM- 476 398  2833387 286 L---------S-GKAKCKAELQKELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPELM- 334 399 15237934 436 V---------S-EKIKCKMALQKELGLPIRFECPMIGFIGRLDYQKGIDLIQTAGPDLM- 484 400  6690399 359 V---------S-EKIKCKMALQKELGLPIRPECPMIGFIGRLDYQKGIDLIQTAGPDLM- 407 401  2829792 425 L---------S-GKVQCKTDLQKELGLPIRPDCPLIGFIGRLDYQKGVDIILSAIFELM- 473 402 15232051 583 L---------HIGKPQCKAALQKYLGLFVRPDVPLIGFIGRLDHQKGVDLIAEAVPWMM- 632 403  3192881 421 LQ--------T-GKPQCKAALQKEMNLPVRDDVPLIGFIGRLDHQKGVDLIAEAIPWMM- 470 404  2833384 543 LQ--------T-GKRQCKAALQRELGLFVREDVPIISFIGRLDHQKGVDLIAEAIPWMM- 592 405  2129898 543 LQ--------T-GKRQCKAALQRELGLPVREDVPIISFIGRLDHQKGVDLIAEAIPWMM- 592 406  6467503 542 LD--------T-GKPQCKTALQNELRFAIPPDVPVIGFIGRLDYQKGVDLIAEAIPWMM- 591 407 14495348 540 VQ--------A-GKQQCKAALQKELGLPVRGDVFVIAFIGRLDHQKGVDLIAEAMPWIA- 589 408  7489711 481 YTNYTFETLDT-GKRQCKAALQRQLGLQVPDDVPLIGFIGRLDHQKGVDIIADAIHWIA- 538 409  8708896 367 L---------AEGKAKCKAALQKELGLPVDPDAPMLGFIGRLDYQKGVDLIRDNYDYIM- 416 410 15384987 428 LD--------T-GKKQCKEALQRQLGLQVRDDVPLIGFIGRLDHQKGVDIIGDAYPWIA- 477 411 15028467 485 LD--------T-GKKQCKEALQRQLGLQVRDDVPLIGFIGRLDHQKGVDIIGDPYPWIA- 534 412  7489710 523 LD--------A-GKRQCKAAJJQRELGLEVRDDVPLLGFIGRLDGQKGVDIIGDYPWIA- 572 413  2833390 579 LQ--------T-GKPQCKAALQKELGLPVRDDVPLIGFIGRLDPQKGVDLIAEAVPWDA- 628 414  7489695 282 LD--------S-GKRQCKEALQRELGLQVRLVPLLGFIGRLDGQKGVEIIAGDAMPWIV- 331 415  8953573 589 LD--------S-GKRQCKEALQRELGLQVRGDVPLLGFIGRLDGQKGVEIIADAMPWIV- 638 416  8953571 590 LD--------S-GKRQCKEALQRELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWIV- 639 417  7529653 590 LD--------S-GKRQCKEALQRELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWIV- 639 418 16265834 601 LD--------S-SKPRCKAALQRELGLEVPDDVPLIGFIGRLDGQKGVDIIGDAMPWIA- 650 419  5825480 590 LD--------S-GKRQCKEALQRELGLQVRNVPLLGFIGRLDGQKGVEIIADDAMPWIV- 639 420  2833388 377 M---------D-AKPLLKEALQAEVGLPVDRNVPLIGFIGRLEEQKGSDIFVAAISQLV- 425 421  5441242 374 VK--------E-AKFLLKEALQAEVGLPVNRDIFLIGFIGRLEEQKGSDILVEAIPKFI- 423 422 12003285 373 M---------D-GKPLLKEALQAEVGLPVDRNVPLVGFIGRLEEQKGSDILVPALHKFI- 421 423   267196 376 M---------D-AKPLLKEALQAAVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKFI- 424 424   228210 376 M---------D-AKPLLKEAWQAAVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKFI- 424 425   602594 376 M---------D-AKPLLKEALQAAVGLPVDKKVPLIGFIGRLEEQKGSDILVAAINKFI- 424 426 16716335 358 VY--------A-GKAAAKEALQAELGLPVDPTAPLFAFIGRLEEQKGVDIILAALPKIIA 408 427  6136121 377 M---------D-AKPLLKEALQAAVGLPVDKNIPVIGFIGRLEEQKGSDILVAAISKFV- 425 428 15223331 378 V---------TDAKPLIKEALQAAVGLPVDRDVPVIGFIGRLEEQKGSDILVEAISKFM- 427 429 15626365 382 L---------E-GKALLKEELQAEVGLPVDKNVPLIAFIGRLEEQKGSDILVEAIPQFI- 430 430  3832512 375 V---------TEAKAILKEALQAEVGLPVDRNIPVIGFIGRLEEQKGSDILVESIPKFI- 424 431  2833381 377 M---------Q-AKPLLKEALQAAVGLPVDRNIPLIGFIGRLEEQKGSDILYAAISKFI- 425 432 15637079 377 M---------Q-AKPLLKEALQAAVGLPVDRNIPLIGFIGRLEEQKGSDILYAAISKFI- 425 433  2833383 371 V---------TEAKPLLKGTLQAEIGLFVDSSIPLIGFIGRLEEQKGSDILVEAIAKFA- 420 434   297424 378 I---------E-AKALNKEALQAEAGLPVDRKIPLIAFIGRLEEQKGSDVMAAAIPELM- 426 435    82478 378 I---------E-AKALNKEALQAEAGLFVDRKIPLIAFIGRLEEQKGPDVMAAAIPELM- 426 436  2833385 377 V---------E-AKALNKEALQAEVGLFVDRKIPLVAFIGRLEEQKGPDVMMAAIPLLM- 425 437  2833382 378 I---------E-AKALNKEALQAEAGLPVDRKIPLIAFIGRLEEQKGPDVMAAAIPELM- 426 387 Maize SSI 474 REDVQFVMLGSGDPELEDWMRSTESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 533 388  7489712 474 REDVQFVMLGSGDPELEDWMRSTESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 533 389 12019656 481 RDDVQFVMLGSGDPELEDWMRSTESDFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 540 390  1549232 475 RDNIQFVMLGSGDPGFEGWMRSTESGYRDKFRGWVGFSVPVSNRITAGCDILLMPSRFEP 534 391  2833377 475 RDNIQFVMLGSGDPGFEGWMRSTESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 534 392  5295947 475 RDNIQFVMLGSGDPGFEGWMRSTESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 534 393  9369336 481 REDVQFVMLGSGDPIFEGWMRSTESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 540 394  6103327 481 REDVQFVMLGSGDPIFEGWMRSTESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEF 540 395  9369334 481 REDVQFVMLGSGDPIFEGNMRSTESSYKDKFRGNVGFSVPVSHRITAGCDILLMPSRFEP 540 396  5880466 481 REDVQFVMLGSGDPIFEGWMRSTESSYKDKFRGWVGFSVPVSHRITAGCDILLMFSRFEP 540 397  7188796 477 REDVQFVMLGSGDFVFEGWMRSTESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 536 398  2833387 335 REDVQFVMLGSGDPIFEGWMRSTESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEP 394 399 15237934 485 VDDIQFVMLGSGDPKYESWMRSMEETYRDKFRGWVGFNVPISHRITAGCDILLMPSRFEP 544 400  6690399 408 VDDIQFVMLGSGDFKYESWMRSMEETYRDKFRGWVGFNVFISHRITAGCDILLMPSRFEP 467 401  2829792 474 QNDVQVVMLGSGEKQYEDWMRHTENLFKDKFRAWVGFNVPVSHRITAGCDILLMPSRFEP 533 402 15232051 633 SQDVQLVMLGTGRPDLEEVLRQMEHQYRDKAAGWVGFSVKTAHRITAGADILLMPSRFEP 692 403  3192881 471 GQDVQLVMLGTGRPDLEQMLKQIEGQYGDKVRGWVGFSVKTAHRITAGADILLMPSRFEP 530 404  2833384 593 SHDVQLVMLGTGRADLEQMLKEFEAQHCDKIRSWVGFSVKIAHRITAGSDILLMPSRFEP 652 405  2129898 593 SHDVQLVMLGTGRADLEQMLKEFEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEP 652 406  6467503 592 GQDVQLVMLGTGRQDLEEMLRQFENQHRDKVRGWVGFSVKTAHRITAGADILLMPSRFEP 651 407 14495348 590 GQDVQLIMLGTGRQDLEDTLRRLESQHYDRVRGWVGFSIRLAHRITAGADILLMPSRFEP 649 408  7489711 539 GQDVQLVMLGTGRADLEDMLRRFESSEHSDKVRAWVGFSVPLAHRITAGDILLMPSRFEP 598 409  8708896 417 GEKCQLVMLGSGRQDLEDALPLMENRNKNQCRGWVGFSNKMAHRITAAADILLMPSRFEP 476 410 15384987 478 GQDVQVVMLGTGRPDLEEMLRRFESEHNDKVRGWVGFSVLAHRITAAGADVLLMPSRFEP 537 411 15028467 535 GQDVQVVMLGTGRPDLEEMLRRFESEHNDKVRGWVGFSVQLAERITAGADVLLMPSRFEP 594 412  7489710 573 GQDVQLVMLGTGRADLERMLQHLEREHPNKVRGWVGFSVQLAERITAGADVLVMPSRFEP 632 413  2833390 629 GQDVQLVMLGTGRRDLEQMLRQFECQHNDKIRGWVGFSVKTSHRITAGADVLLMFSRFEP 688 414  7489695 332 SQDVQLVMLGTGRHDLESMLQHFEREHHDKIRGWVGFSVRLAHRITAGADVLLMPSRFEP 391 415  8953573 639 SQDVQLVMLGTGRHDLEGMLRLHFEREHHDKRGWVGFSVRLAHRITAGADMLLMPSRFEP 698 416  8953571 640 SQDVQLVMLGTGRHDLESMLRLFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEP 699 417  7529653 640 SQDVQLVMLGTGRHDLESMLQHFEREHHDKVRGWVGFSVRLAHRITAGALDALMPSRFEP 699 418 16265834 651 GQDVQLVLLGSGRRDLEVMLQRFEAQHNSKVRGWVGFSVKLAHRITAGADVLVMPSRFEP 710 419  5825480 640 SQDVQLVMLGTGRHDLESMLRHFEREHNDKVRGWVGFSVRLAHRITAGADALLMPSRFEP 699 420  2833388 426 EHNVQIVILGTGKKKFEKQIEHLEVIYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEP 485 421  5441242 424 DQNVQIIILGTGKKSMEKQIEQLEEIYPEKARGIAKFDGPLAHKIIAGSDFIMIPSRFEP 483 422 12003285 422 EMDVQVVILGTGKKEFEKQIEQLEELYPGKAVGVAKFNVPLAHKITAGADFMLVPSRFEP 481 423   267196 425 GLDVQIVVLGTGKKEFEQEIEQLEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEP 484 424   228210 425 GLDVQIVVLGTGKKEFEQEIEQLEVLYPGKVKGVAKFNVPLAHMITAGADFMLVPSRFEP 484 425   602594 425 GLDVQIVVLGTGKKEFEQEIEQLEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEP 484 426 16716335 409 TPKVQIAILGTGKAAYEKLVNAIGTKYKGRAKGVVKFSAPLAHMLTAGADFNLVPSRFEP 468 427  6136121 426 GLDVQIIILGTGKKKFEQQIQELEVLYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEP 485 428 15223331 428 GLNVQMVILGTGKKKMEAQILELEEKFPGKAVGVAKFNVPLAHMITAGADFIIVPSRFEP 487 429 15626365 431 KENVQIVALGTGKKEMEKQLQQLEISYPDKARGVAKFNVPLAHMMIAGADFILIPSRFEP 490 430  3832512 425 DQNVQIIVLGTGKKIMEKQILEQLEVTYPGKAGVAKFNSPLAHKIIAGADFIVIPSRFEP 484 431  2833381 426 SMDVQILILGTGKKKFEQQIEQLEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEP 485 432 15637079 426 SMDVQILILGTGKKKFEQQIEQLEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEP 485 433  2833383 421 DENVQIVVLGTGKKIMEKQIEVLEEKYPGKAIGITKFNSPLAHKIIAGADFIVIPSRFEP 480 434   297424 427 QEDVQIVLLGTGKKKFEKLLKSMEEKYPGKVRAVVKFNAPLAHLIMAGADVLAVPSRFEP 486 435    82478 427 QEDVQIVLLGTGKKKFEKILKSMEEKYPGKVRAVVKFNAPLAHLIMAGADVLAVPSRFEF 486 436  2833385 426 EEDIQIVLLGTGKKKFERALMSAEEKYPDKVPAVVKFNAALAHHIMAGADLLAVTSRFEP 485 437  2833382 427 QEDVQIVLLGTGKKKFEKLLKSMEEKYPGKVPAVVKFNAPLAHLIMAGIDVLAVFSRFEP 486 387 Maize SSI 534 CGLNQLYAMQYGTVPVVHATGGLRDTV-ENFNPF-GENG-EQGTGWAFAFLTTENMFVDI 590 388  7489712 534 CGLNQLYAMQYGTVPVVHATGGLRDTV-ENFNPF-GENG-EQGTGWAFAPLTTENMFVDI 590 389 12019656 541 CGLNQLYAMQYGTVPVVHATGGLRDTV-ENFNPF-GENG-EQGTGWAFAPLTTENMFVDI 597 390  1549232 535 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ENFNPF-AEKG-EQGTGWAFSPLTIEKNAVGI 591 391  2833377 535 CGLNQLYAMQYGTVPVVUGTGGLRDTV-ENFNPF-AEKG-EQGTGWAFSPLTIEKNAVGI 591 392  5295947 535 CGLNQLYANQYGTVPVVHGTGGLRDTV-ENFNPF-AEKG-EQGTGWAFSPLTIEK---GI 588 393  9369336 541 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVEKM     593 394  6103327 541 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVDKM     593 395  9369334 541 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVDKM     593 396  5880466 541 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVDKM     593 397  7188796 537 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVDKM     589 398  2833387 395 CGLNQLYAMQYGTVPVVHGTGGLRDTV-ETFNPF-GAKG-EEGTGWAFSPLTVDKM     447 399 15237934 545 CGLNQLYAMRYGTIPVVHGTGGLPDTV-ENFNPYAEGGA-GTGTGWVFTPLSKDSM     598 400  6690399 468 CGLNQLYAMRYGTIPVVHGTGGLRDTV-ENFNPYAEGGA-GAGTGWVFTPLSKDSM     521 401  2829792 534 CGLNQLYAMRYGTIPIVHSTGGLRDTV-KDFNPY-AQEGIGEGTGWTFSPLTSEKL     587 402 15232051 693 CGLNQLYAMNYGTIPVVHAVGGLRDTV-QQFDPY-SET----GLGWTFDSAEAGKLIHAL 746 403  3192881 531 CGLNQLYAMSYGTVPVVHAVGGLRDTV-QPFDPF-NES----GYGWTFGRAEANQLIDAL 584 404  2833384 653 CGLNQLYANSYGTVPVVHGVGGLRDTV-QPFNPF-DES----GVGWTFDRAEANKLMAAL 706 405  2129898 653 CGLNQLYANSYGTVPVVHGVGGLRDTV-QPFNPF-DES----GVGWTFDRAEANKLMAAL 706 406  6467503 652 CGLNQLYAPMYGTIPVVRAVGGLRDTV-QPFDPF-NES----GLGWTFDSAESHKLIHAL 705 407 14495348 650 CGLNQLYAMMYGTVPVVHAVGGLRDTV-EHYNPY-EES----GLGWTFEKAEARNLIDAL 703 408  7489711 599 CGLNQLYAMAYGTVPVVHAVGGLRDTV-APFDPF-NDT----GLGWTFDRAEANRMIDAL 652 409  8708896 477 CGLNQLYAMAYGTVPIVHSVGGLRDTV-KQYSPF--EN---VGTGWVF             518 410 15384987 538 CGLNQLYAMAYGTVFVVHAVGGLRDTV-APFDPF-ADT----GLGWTFDRAEANRMIDAL 591 411 15028467 595 CGLNQLYAMAYGTVFVVHAVGGLRDTV-APFDPF-ADT----GLGWTFDRAEANRMIDAL 648 412  7489710 633 CGLNQLYAMAYGTVPVVHAVGGLRDTV-APFDPF----G-DAGLGWTFDRAEANKLIEAL 686 413  2833390 689 CALNQLYAMAYGTVPVVHAVGGLRDTV-QPFDP                            720 414  7489695 392 CGLNQLYAMAYGTVPVVHAVGGLRDTV-PPFDPF-NHS----GLGWTFDRAEAHKLIEAL 445 415  8953573 699 CGLNQLYAMAYGTVPVVHAVGGLRDTV-PPFDPF-NHS----GLGWTFDRAEAQKLIEAL 752 416  8953571 700 CGLNQLYAMAYGTVPVVHAVGGLRDTV-PPFDPF-NHS----GLGWTFDRAEAHKLIEAL 753 417  7529653 700 CGLNQLYAMAYGTVPVVHAVGGLRDTV-PPFDPF-NHS----GLGWTFDRAEAHKLIEAL 753 418 16265834 711 CGLNQLYAMAYGTVPVVHAVGGLRDTM-SAFDPF-EDT----GLGWTFDRAEFHKLIEAL 764 419  5825480 700 CGLNQLYAMAYGTVPVVHAVGGVRDTV-PPFDPF-NNS----GLGWTFDPAEAHKLIEAL 753 420  2833388 486 CGLIQLHAMRYGTVPIVASTGGLRDTV-K-----------EGYTGFQMGALHVECDKIDS 533 421  5441242 484 CGLVQLHSMPYGTVPIVSSTGGLVDTVQEGFTGF                           517 422 12003285 482 CGLIQLHANRYGTIPICASTGGLVDTVKEGFTGF                           515 423   267196 485 CGLIQLHAMRYGTVPICASTGGLVDTV-K                                512 424   228210 485 CGLIQLHAMRYGTVPICASTGGLVDTV-K                                512 425   602594 485 CGLIQLHAMRYGTVPICASTGGLVDTV-K                                512 426 16716335 469 CGLIQLHANHYGTVPVVASTGGLVDTV-K                                496 427  6136121 486 CGLIQLHAMRYGTIPICASTGGLVDTVTEGFTGF                           519 428 15223331 488 CGLIQLHANRYGTVPIVASTGGLVDTV-KD                               516 429 15626365 491 CGLIQLQAIVIRYGTVPIVASTGGLVDTVKEGFTGF                         524 430  3832512 485 CGLVQLHANFYGTVPIVSSTGGLVDTV-K-----------EGYTGFHVGAFSVECEAVDP 532 431  2833381 486 CGLIQLHAMRYGTPCICASTGGLVDTV-K                                513 432 15637079 486 CGLIQLHAMRYGTPCICASTGGLVDTV-K                                513 433  2833383 481 CGLVQLHAMPYGTVPIVSSTGGLVDTV-K-----------EGYTGFHAGPFDVECEDVD  527 434   297424 487 CGLIQLQGMRYGTPCACASTGGLVDTV                                  513 435    82478 487 CGLIQLQGMRYGTACACASTGGLVDTV                                  513 436  2833385 486 CGLIQLQGMRYGTPCACASTGGLVDTI                                  512 437  2833382 487 CGLIQLQGMRYGTPCACASTGGLVDTV                                  513

[0389] TABLE XVII Maize soluble starch synthase I (SSI) “CTEND” Domain Alignments with other similar proteins SEQ Acces- a. Id. sion a.a a. No. Number # (start)       Sequence       end # 438 MaizeSSI 591 ANCNIYIQGTQVLLGRANEARHVKRLHVGPCR 622 439  7489712 591 ANCNIYIQGTQVLLGRANEARHVKRLHVGPCR 622 440 12019656 598 ANCNFDIQGAQIFLGRANEEGHVKRLIWGPCR 629 441  1549232 592 ADGNFDIQGTQVLLGGSNEARHVKRLYMGPCR 623 442  2833377 592 ADGNFDIQGTQVLLGGSNEARHVKRLYMGPCR 623 443  5295947 589 ADGNFDIQGTQVLLGGSNEARHVKRLYMGPCR 620 444 15232051 747 GNC 749 445  3192881 585 GNC 587 446  2833384 707 WNC 709 447  2129898 707 WNC 709 448  6467503 706 GHC 708 449 14495348 704 GHC 706 450  7489711 653 SHC 655 451 15384987 592 GHC 594 452 15028467 649 GHC 651 453  7489710 687 RHC 689 454  7489695 446 GHC 448 455  8953573 753 GHC 755 456  8953571 754 GHC 756 457  7529653 754 GHC 756 458 16265834 765 GHC 767 459  5825480 754 GHC 756 460  2833388 534 ADVAAIVKTVARALG 548 461  3832512 533 AD 534

[0390] TABLE XVIII Identities of the Accession Numbers used in Tables. XIV-XVII. Accession Brief Description of sequences Id. producing significant alignments score E-value gi|7489712|pir||T01414 ADPglucose - starch glucosyltransfera . . . 1189 0.0 gi|12019656|gb|AAD45815.2| (AF168786) soluble starch syntha . . . 1145 0.0 gi|1549232|dbj|BAA07396.1| (D38221) SSS1 [Oryza sativa] >gi . . . 998 0.0 gi|2833377|sp|Q40739|UGS2_ORYSA Soluble glycogen [starch] s . . . 996 0.0 gi|5295947|dbj|BAA81848.1| (AB026295) ESTs AU075322 (C11109) . . . 992 0.0 gi|9369336|emb|CAB99210.1| (AJ292522) starch synthase I-2 [. . . 953 0.0 gi|6103327|gb|AAF03557.1| (AF091802) starch synthase I [Aeg . . . 953 0.0 gi|9369334|emb|CAB99209.1| (AJ292521) starch synthase I-1 [. . . 952 0.0 gi|5880466|gb|AAD54661.1| (AF091803) starch synthase I [Tri . . . 951 0.0 gi|7188796|gb|AAF37876.1|AF234163_1 (AF234163) starch synth . . . 949 0.0 gi|2833387|sp|Q43654|UGS2_WHEAT Soluble glycogen [starch] s . . . 884 0.0 gi|15237934|ref|NP 197818.1| (NM_122336) soluble starch syn . . . 744 0.0 gi|6690399|gb|AAF24126.1|AF121673_1 (AF121673) soluble star . . . 741 0.0 gi|2829792|sp|P93568|UGS2_SOLTU Soluble glycogen [starch] s . . . 724 0.0 gi|15232051|ref|NP_186767.1| (NM_110984) putative glycogen . . . 447 e−124 gi|3192881|gb|AAC19119.1| (AF068834) starch synthase [Ipomo . . . 443 e−123 gi|2833384|sp|Q43093|UGS3_PEA Glycogen [starch] synthase, c . . . 431 e−120 gi|2129898|pir||S61505 UDPglucose - starch glucosyltransfera . . . 431 e−119 gi|6467503|gb|AAF13168.1|AF173900_1 (AF173900) granule boun . . . 430 e−119 gi|14495348|gb|AAK64284.1|AF383878_1 (AF383878) soluble sta . . . 426 e−118 gi|7489711|pir||T01209 ADPglucose - starch glucosyltransfera . . . 421 e−117 gi|8708896|gb|AAC17970.2| (AF026421) soluble starch synthas . . . 419 e−116 gi|15384987|emb|CAC59826.1| (AJ308110) soluble starch synth . . . 419 e−116 gi|15028467|gb|AAK81729.1|AF395537_1 (AF395537) soluble sta . . . 416 e−115 gi|7489710|pir||T01208 ADPglucose - starch glucosyltransfera . . . 414 e−114 gi|2833390|sp|Q43847|UGS3_SOLTU Glycogen [starch] synthase, . . . 410 e−113 gi|7489695|pir||T06798 probable starch synthase (EC 2.4.1.— . . . 405 e−112 gi|8953573|emb|CAB96627.1| (AJ269504) starch synthase IIa-3 . . . 388 e−107 gi|8953571|emb|CAB96626.1| (AJ269503) starch synthase IIa-2 . . . 388 e−107 gi|7529653|emb|CAB86618.1| (AJ269502) starch synthase IIa-1 . . . 388 e−107 gi|16265834|gb|AAL16661.1|AF419099_1 (AF419099) putative so . . . 387 e−106 gi|5825480|gb|AAD53263.1|AF155217_1 (AF155217) starch synth . . . 387 e−106 gi|2833388|sp|Q43784|UGST_MANES Granule-bound glycogen [sta . . . 340 3e−92 gi|5441242|dbj|BAA82346.1| (AB029546) granule-bound starch . . . 334 2e−90 gi|12003285|gb|AAG43519.1| AF210699_1 (AF210699) granule-bou . . . 325 7e−88 gi|267196|sp|Q00775|UGST_SOLTU Granule-bound glycogen [star . . . 325 8e−88 gi|228210|prf||1718316A granule-bound starch synthase [Sola . . . 324 2e−87 gi|602594|emb|CAA58220.1| (X83220) starch (bacterial glycog . . . 324 2e−87 gi|16716335|gb|AAC17969.3| (AF026420) granule-bound starch . . . 322 7e−87 gi|6136121|sp|O82627|UGST_ANTMA Granule-bound glycogen [sta . . . 321 2e−86 gi|15223331|ref|NP_174566.1| (NM_103023) starch synthase, p . . . 317 3e−85 gi|15626365|emb|CAC69955.1| (AJ345045) granule-bound starch . . . 315 1e−84 gi|3832512|gb|AAC70779.1| (AF097922) granule-bound glycogen . . . 313 4e−84 gi|2833381|sp|Q42857|UGST_IPOBA Granule-bound glycogen [sta . . . 311 9e−84 gi|15637079|dbj|BAB68126.1| (AB071604) granule-bound starch . . . 311 1e−83 gi|2833383|sp|Q43092|UGST_PEA Granule-bound glycogen [starc . . . 310 4e−83 gi|297424|emb|CAA46294.1| (X65183) glycogen (starch) syntha . . . 303 4e−81 gi|82478|pir||JQ0703 UDPglucose - starch glucosyltransferase . . . 303 5e−81 gi|2833385|sp|Q43134|UGST_SORBI Granule-bound glycogen [sta . . . 303 5e−81 gi|2833382|sp|Q42968|UGST_ORYGL Granule-bound glycogen [sta . . . 302 6e−81 gi|136758|sp|P19395|UGST_ORYSA Granule-bound glycogen [star . . . 302 6e−81 gi|15900991|ref|NP_345595.1| (NC_003028) glycogen synthase . . . 302 6e−81 gi|7798551|gb|AAC61675.2| (AF031162) granule-bound starch s . . . 301 1e−80 gi|15903076|ref|NP_358626.1| (NC_003098) Glycogen synthase . . . 301 1e−80 gi|136757|sp|P04713|UGST_MAIZE Granule-bound glycogen [star . . . 300 2e−80 gi|4760582|dbj|BAA77351.1| (AB019623) starch synthase (GBSS . . . 300 4e−80 gi|11037536|gb|AAG27624.1|AF286320_1 (AF286320) granule bou . . . 300 4e−80 gi|6624287|dbj|BAA88512.1| (AB029064) starch synthase (GBSS . . . 296 3e−79 gi|6492245|gb|AAF14233.1|AF109395_1 (AF109395) granule-boun . . . 296 4e−79 gi|6624281|dbj|BAA88509.1| (AB029061) starch synthase (GBSS . . . 296 4e−79 gi|297422|emb|CAA45472.1| (X64108) starch granule-bound sta . . . 295 9e−79 gi|6624283|dbj|BAA88510.1| (AB029062) starch synthase (GBSS . . . 294 1e−78 gi|6624285|dbj|BAA88511.1| (AB029063) starch synthase (GBSS . . . 294 2e−78 gi|4588609|gb|AAD26156.1|AF113844_1 (AF113844) granule-boun . . . 294 2e−78 gi|18652407|gb|AAL77109.1|AF474373_6 (AF474373) granule-bou . . . 294 2e−78 gi|136755|sp|P09842|UGST_HORVU Granule-bound glycogen [star . . . 293 3e−78 gi|4760584|dbj|BAA77352.1| (AB019624) starch synthase (GBSS . . . 293 4e−78 gi|6318540|gb|AAF06937.1|AF110374_1 (AF110374) granule-boun . . . 293 5e−78 gi|17736918|gb|AAL41028.1| (AF250137) mutant granule bound . . . 292 7e−78 gi|6318538|gb|AAF06936.1|AF110373_1 (AF110373) granule-boun . . . 290 4e−77 gi|4760580|dbj|BAA77350.1| (AB019622) starch synthase (GBSS . . . 290 4e−77 gi|136765|sp|P27736|UGST_WHEAT Granule-bound glycogen [star . . . 288 2e−76 gi|15672681|ref|NP_266855.1| (NC_002662) glycogen synthase . . . 287 3e−76 gi|17366711|sp|Q9CHM9|GLGA_LACLA Glycogen synthase (Starch . . . 286 4e−76 gi|18139611|gb|AAL58572.1| (AY069940) granule binding starc . . . 285 1e−75 gi|16080147|ref|NP_390973.1| (NC_000964) starch (bacterial . . . 281 1e−74 gi|4588607|gb|AAD26155.1|AF113843_1 (AF113843) granule-boun . . . 278 1e−73 gi|7484400|pir| |T07924 probable starch synthase (EC 2.4.1.- . . . 277 2e−73 gi|2811062|sp|O08328|GLGA_BACST Glycogen synthase (Starch [. . . 270 3e−71 gi|18309046|ref|NP_560980.1| (NC_003366) glycogen synthase . . . 263 5e−69 gi|15895507|ref|NP_348856.1| (NC_003030) Glycogen synthase, . . . 256 6e−67 gi|15966599|ref|NP_386952.1| (NC_003047) PROBABLE GLYCOGEN . . . 248 1e−64 gi|15643657|ref|NP_228703.1| (NC_000853) glycogen synthase . . . 247 3e−64 gi|16766821|ref|NP_462436.1| (NC_003197) glycogen synthase . . . 242 1e−62 gi|15613648|ref|NP_241951.1| (NC_002570) starch (bacterial . . . 241 2e−62 gi|16762766|ref|NP_458383.1| (NC_003198) glycogen synthase . . . 240 3e−62 gi|15641730|ref|NP_231362.1| (NC_002505) glycogen synthase . . . 239 5e−62 gi|15803938|ref|NP_289974.1| (NC_002655) glycogen synthase . . . 237 3e−61 gi|16124067|ref|NP_407380.1| (NC_003143) glycogen synthase . . . 235 1e−60 gi|15890897|ref|NP_356569.1| (NC_003063) AGR_L_1562p [Agrob . . . 228 1e−58 gi|16119514|ref|NP_396220.1| (NC_003064) AGR_pAT_410p [Agro . . . 226 8e−58 gi|17938870|ref|NP_535658.1| (NC_003306) glycogen synthase . . . 225 9e−58 gi|9587341|gb|AAF89272.1|AF285997_1 (AF285997) granule-boun . . . 222 1e−56 gi|9587301|gb|AAF89252.1|AF285977_1 (AF285977) granule-boun . . . 221 1e−56 gi|9587321|gb|AAF89262.1|AF285987_1 (AF285987) granule-boun . . . 221 2e−56 gi|9587293|gb|AAF89248.1|AF285973_1 (AF285973) granule-boun . . . 221 2e−56 gi|15606118|ref|NP_213495.1| (NC_000918) glycogen synthase . . . 220 3e−56 gi|9587343|gb|AAF89273.1|AF285998_1 (AF285998) granule-boun . . . 220 3e−56 gi|15602409|ref|NP_245481.1| (NC_002663) GlgA [Pasteurella . . . 219 7e−56 gi|9587317|gb|AAF89260.1|AF285985_1 (AF285985) granule-boun . . . 218 1e−55

[0391] Maize Soluble Starch Synthase IIa (SSIIa) Accession: AF019296 NID:       g2811133            Mol. wt. (calc) = 80156    Residues = 732 1 M S S A A V S S S S S T F F L A L A S A S P G G R R R A R V SEQ. ID. No. 462 31 G S S P F H T G A S L S F A F W A P P S P P R A P R D A A L 61 V R A E A E A G G K D A P P E R S G D A A R L P R A R R N A 91 V S K R R D P L Q P V G R Y G S A T G N T A R T G A A S C Q 121 N A A L A D V E I K S I V A A P P T S I V K F P A P G Y R M 151 I L P S G D I A P E T V L P A P K P L H E S P A V D G D S N 181 G I A P P T V E P L V Q E A T W D F K K Y I G F D E P D E A 211 K D D S R V G A D D A G S F E H Y G D N D S G P L A G E N V 241 M N V I V V A A E C S P W C K T G G L G D V V G A L P K A L 271 A R R G H R V M V V V P R Y G D Y V E A F D M G I R K Y Y K 301 A A G Q D L E V N Y F H A F I D G V D F V F I D A P L F R H 331 R Q D D I Y G G S R Q E I M K R M T L F C K V A V E V P W H 361 V P C G G V C Y G D G N L V F I A N D W H T A L L P V Y L K 391 A Y Y R D H G L M Q Y T R S V L V I H N I A H Q Q R G P V D 421 E F P Y M D L P E H Y L Q H F E L Y D P V G G E H A N I F A 451 A G L K M A D R V V T V S R G Y L W E L K T V E G G W G L H 481 D I I R S N D W K I N G I V N G I D H Q E W N P K V D V H L 511 R S D G Y T N Y S L E T L D A G K R Q C K A A L Q R E L G L 541 E V R D D V P L L G F I G R L D G Q K G V D I I G D A M P W 571 I A G Q D V Q L V M L G T G R A D L E R M L Q H L E R E H P 601 N K V R G W V G F S V P M A H R I T A G A D V L V M P S R F 631 E P C G L N Q L Y A M A Y G T V P V V H A V G G L R D T V A 661 P F D P F G D A G L G W T F D R A E A N K L I E A L R H C L 691 D T Y R K Y G E S W K S L Q A R G M S Q D L S W D H A A E L 721 Y E D V L V K A K Y Q W

[0392] TABLE XIX Maize soluble starch synthase IIa (SSIIa) Alignments with other similar proteins—Transit Peptide SEQ Accession a.a a.a. Id.No. Number # (start)                Sequence                ending # 463 MAIZE SSIIa 34 PFHTGXXXXXXXXXXXXXXXXXXXXXXXVRAEAEAGGKDAPPER--SGDAARLPRARRBAV 91 464  7489710 34 PFHTGASLSFAFWAPPSPPPRAPRDAALVRAEAEAGGKDAPPER--SGDAARLPRARRNAV 91 465  8953573 101                                DAAEGGAPSPPAP--RQEDARLPSMNGMPV 128 466  8953571 102                                DAAEGGAPAPPAP--RQDAARPPSMNGTPV 129 467  5825480 102                                DAAEGGAPAPPAP--RQDAARPPSMNGTPV 129 468  7529653 102                                DAAEGGGPSPPAA--RQDAARPPSMNGMPV 129 469 16265834 78                               AAVERAGEDDDEEEEFSSGAWQPPRSRRGGV 108 470  7489711 38                                             --SGAELRLHWARRGPP 52 471  7188796 21                                                      PAARATAC 28 472  2833377 16                                        APQVR--PGRRLRLQRVRRRCV 35 473  1549232 16                                        APQVR--PGRRLRLQRVRRRCV 35 474  5295947 16                                        APQVR--PGRRLRLQRVRRRCV 35

[0393] TABLE XX Maize soluble starch synthase ha (SSIIa) “GLASS” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start) Sequence end # 475 MaizeSSIIa 92 S---K-RRDPLQPVG-RYGSATGNTAR-------------------TG---A-------- 116 476  7489710 92 S---K-RRDPLQPVG-RYGSATGNTAR-------------------TG---A-------- 116 477  8953573 129 N---G-ENKSTGGGGATKDSGLPAPAR-------------------AP---Q-------- 154 478  8953571 130 N---G-ENKSTGGGGATKDSGLPAPAR-------------------AP---H-------- 155 479  5825480 130 N---G-ENKSTGGGGATKDSGLPAPAR-------------------AP---H-------- 155 480  7529653 130 N---G-ENKSTGGGGATKDSGLPTPAR-------------------AP---H-------- 155 481 16265834 109 GKVLK-RRGTVPPVG-RYGSG-GDAARVRGAAAPAPAPTQDAASSKNG---ALLSGRDDD 162 482 15028467 67               G-EDGVAKAKTKS-------------------AGSSKA-------- 84 483  7489711 53 Q---D-GAASVRAAA-APAGGESEEAA-------------------KS---S-------- 77 484  5880466 42               G-RY---VAELSR-------------------EG---P-------- 53 485  9369334 42               G-RY---VAELSR-------------------EG---P-------- 53 486  6103327 42               G-RY---VAELSR-------------------EG---P-------- 53 487  7188796 29 V---V-RARLRRVAR-GRYVA--ELSR-------------------EG---P-------- 51 488  2833377 36 A---ELSRDG--------GSAHGPLA---------------------------------- 50 489  1549232 36 A---E-------------------LSR-------------------DG---G-------- 43 490  5295947 36 A---E-------------------LSR-------------------DG---G-------- 43 475 MaizeSSIIa 117 CQNAALADVEIKSI------VAAP--PTSIVKFPAPGY--RMIL---PSGD--I---A-- 158 476  7489710 117 -AS--CQNAA ADVEIKSI-VAAP--PTSIVKFPAPGY--RMIL---PSGD--I---A-- 158 477  8953573 155 -PS--SQNRVPVNGENKAN-VASP--PTSIAEVAAPDP--AATI---SISD--K---A-- 196 478  8953571 156 -PS--TQNRVPVNGENKAN-VASP--PTSIAEVVAPDS--AATI---SISD--K---A-- 197 479  5825480 156 -PS--TQNRVPVNGENKAN-VASP--PTSIAEVVAPDS--AATI---SISD--K---A-- 197 480  7529653 156 -PS--TQNRAPVNGENKAN-VASP--PTSIAEAAASDS--AATI---SISD--K---A-- 197 481 16265834 163 TPA--SRNGSVVTGADKPA-AATP--PVTITKLPAPDS--PVIL---PSVD--K---PQP 207 491 15384987 65                                                       ---A-- 65 482 15028467 85 -VA--VQGSTAKADHVEDS-VSSP-------KYVKPA----VAK---QNGE--VVSRA-- 122 483  7489711 78 -SS--SQAGAVQGSTAKAVDSASP--PNPLTSAPKQSQ--SAANQNGTSGG--S---S-- 123 492 15232051 181            ASVISSSP-VTSPQKPSDVATNGKPWS--SVVA---SSVDPPY---K-- 218 484  5880466 54 -AARPAQQQQL-----------AP--PL------VPGFLAPPPP---APAQ--S---P-- 83 485  9369334 54 -AARPAQQQQL-----------AP--PL------VPGFLAPPPP---APAQ--S---P-- 83 486  6103327 54 -AARPAQQQQL-----------AP--PL------VPGFLAPPPP---APAQ--S---P-- 83 487  7188796 52 -AA--RPAQQL-----------AP--PV------VPGFLAPPPP---APAQ--S---P-- 79 488  2833377 51 --------------------------PAPLVKQP--------VL---PTF---L---V-- 65 489  1549232 44 -SA--QRPLA----------------PAPLVKQP--------VL---PTF---L---V-- 65 490  5295947 44 -SA--QRPLA----------------PAPLVKQP--------VL---PTF---L---V-- 65 475 MaizeSSIIa 159 ------------------PETVLPAPK----------PLHE---S----------PAVDG 177 476  7489710 159 ------------------PETVLPAPK----------PLHE---S----------PAVDG 177 477  8953573 197 ------------------PESVVPAEKAPPSSGSNFVPSAS---A----------PGSDT 225 478  8953571 198 ------------------PESVVPAEK----------PPPS---SGSNFVVSASAPRLDI 226 479  5825480 198 ------------------PESVVPAEK----------PPPS---SGSNFVVSASAPRLDI 226 480  7329653 198 ------------------PESVVPA--------------EE---T----------PPSSG 212 481 16265834 208 EFVIPDATAPAPPPPGSNPRSSAPLPK----------PDNS---E----------FAEDK 244 491 15384987 66 ------------------TKSDAPVFK----------PKVD---PSV--------PASKA 86 482 15028467 123 ------------------TKSDAPVSK----------PKVD---PSV--------PASKA 143 483  7489711 124 ------------------ASTAAPVSG----------PKAD---H----------PSAPV 142 492 15232051 219 ------------------PSSVMTSPE----------KTSDPVTS----------PGKPS 240 484  5880466 84 ------------------APTQPPLPD----------AGVG---E----------LAPDL 102 485  9369334 84 ------------------APTQPPLPD----------AGVG---E----------LAPDL 102 486  6103327 84 ------------------APTQPPLPD----------AGVG---E----------LAPDL 102 487  7188796 80 ------------------APTQPPLPD----------AGVG---E----------LAPDL 98 493  7489712 49                        PAPE----------PLPP---A----------LLAPP 62 488  2833377 66 ------------------PTSTPPAPTQSP-------APAP---T----------PPPLP 87 489  1549232 66 ------------------PTSTPPAPTQSP-------APAP---T----------PPPLP 87 490  5295947 66 ------------------PTSTPPAPTQSP-------APAP---T----------PPPLP 87 475 Maize SSIIa 178 ---DSN-------------------GI--A------P----------------------- 184 476  7489710 178 ---DSN-------------------GI--A------P----------------------- 184 477  8953573 226 ---VSDVELELKKGAVIVKEAPNPKAL--S------P----------------------- 251 478  8953571 227 ---DSDVEPELKKGAVIVEEAPNPKAL--S------P----------------------- 252 479  5825480 227 ---DSDVEPELKKGAVIVEEAPNPKAL--S------P----------------------- 252 480  7529653 213 SNFESS-------------------AS--A------PGSDTVSDVEQELKKGAVVVEEAP 245 481 16265834 245 ---SAK-------------------VVESA------PKPKATR----------------- 259 491 15384987 87 ---EAD-------------------GN--A------------------------------ 92 482 15028467 144 ---EAD-------------------GN--A------------------------------ 149 483  7489711 143 ---TKR-------------------EI--D------A----------------------- 149 492 15232051 241 ---KSR-------------------AG--AFWSDPLP----------------------- 253 484  5880466 103 ---LLE-------------------GI--A------E----------------------- 109 485  9369334 103 ---LLE-------------------GI--A------E----------------------- 109 486  6103327 103 ---LLE-------------------GI--A------E----------------------- 109 487  7188796 99 ---LLE-------------------GI--A------E----------------------- 105 493  7489712 63 ---LVP-------------------GF--L------A----------------------- 69 488  2833377 88 ---DSGV------------------GE--I------E----------------------- 95 489  1549232 88 ---DSGV------------------GE--I------E----------------------- 95 490  5295947 88 ---DSGV------------------GE--I------E----------------------- 95 475 MaizeSSIIa 185 ------PTVEPLVQEATWDFK--KYIGFDEP---DEAKDDSRVGADDAGSFEH-YGDN-- 230 476  7489710 185 ------PTVEPLVQEATWDFK--KYIGFDEP---DEAKDDSRVGADDAGSFEH-YGDN-- 230 477  8953573 252 ------PAA-PAVQQDLWDFK--KYIGFEEP---VEACDDGPAVALDAGSFEH-HQNH-- 296 478  8953571 253 ------PAA-PAVQEDLWDFK--KYIGFEEP---VEAKDDGWAVADDAGSFEH-HQNH-- 297 479  5825480 253 ------PAA-PAVQEDLWDFK--KYIGFEEP---VEAKDDGWAVADDAGSFEH-HQNH-- 297 480  7529653 246 KPKALSPPAAPAVQEDLWDFK--KYIGFEEP---VEAKDDGRAVADDAGSFEH-HQNH-- 297 481 16265834 260 ------SSPIPAVEEETWDFK--KYFDLNEPDAAEDGDDDDDWADSDASDSEI-DQDD-- 308 491 15384987 93 ---------QAVESKAALDKK--EDVGVAEP---LEAKADAGGDAGAVSSADD-SENK-- 135 482 15028467 150 ---------QAVESKAALDKK--EDVGVAEP---LEAKADAGGDAGAVSSADD-SENK-- 192 483  7489711 150 ------SAVKP--EPAGDDARPVESIGIAEP---VDAKADAAPATDAAASAPYDREDN-- 196 494  2833384 217             IRTSSLKFE--NFEGANEP--------SSKEVANEAENFES-GGEK-- 251 495  2129898 217             IRTSSLKFE--NFEGANEP--------SSKEVANEAENFES-GGEK-- 251 496 15232051 254 ------SYLTKAPQTSTMKTE--KYVE-KTP---DVASSETNEPGKD---------EE-- 290 497  3192881 107                             DHR---ESSSKEIDVGTEDPVN-----EDL-- 128 498  2833390 284                                                         DE-- 285 499 14495348 247                                                          D-- 247 484  5880466 110 ------DSIDSIIVAASEQDS--EIMDANEQ---PQAK---------------------- 136 485  9369334 110 ------DSIDSIIVAASEQDS--EIMDANEQ---PQAK---------------------- 136 486  6103327 110 ------DSIDSIIVAASEQDS--EIMDANEQ---PQAK---------------------- 136 487  7188796 106 ------DSIDTIVVAAS--------------------EQDSEI------------MDA-- 125 493  7489712 70 ------PPAEPTGEPAS--------TPPPVP---DAGLGD--LGLEPEGIAEG-SIDNTV 109 488  2833377 96 ------PDLEGLTEDSI-DKT--IFVASEQE---SEIMDVKEQA---------------- 127 489  1549232 96 ------PDLEGLTEDSI-DKT--IFVASEQE---SEIMDVKEQA---------------- 127 490  5295947 96 ------PDLEGLTEDSI-DKT--IFVASEQE---SEIMDVKEQA---------------- 127 500  6136121 54                                          RNNAKQSRSLVK-KTDN-- 69 501 15637079 65                                                         EN-- 66 475 Maize SSIIa 231 ------DS--GPLAGEN------V-----MNVIVVAAECSPWCKTGGLGDVVGALPKALA 271 476  7489710 231 ------DS--GPLAGEN------V-----MNVIVVAAECSPWCKTGGLGDVVGALPKALA 271 477  8953573 297 ------DS--GPLAGEN------V-----MNVVVVAAECSPWCKTGGLGDVAGALPKALA 337 478  8953571 298 ------DS--GPLAGEN------V-----MNVVVVAAECSPWCKTGGLGDVAGALPKALA 338 479  5825480 298 ------DS--GPLAGEN------V-----MNVVVVAAECSPWCKTGGLGDVAGALPKALA 338 480  7529653 298 ------DS--GPLAGEN------V-----MNVVVVAAECSPWCKTGGLGDVAGALPKALA 338 481 16265834 309 ------DS--GPLAGEN------V-----MNVIVVAAECSPWCKTGGLGDVAGALPKALA 349 502  7489695 1                               NVVVVAAECSPWCKTGGLGDVAGAIPKALA 30 491 15384987 136 ------ES--GPLAGPN------V-----MNVIVVASECSPFCKTCGLGDVVGALPKALA 176 482 15028467 193 ------ES--GPLAGPN------V-----MNVIVVASECSPFCKTGGLGDVVGALPKALA 233 483  7489711 197 ------EP--GPLAGPN------V-----MNVVVVASECAPFCKTGGLGDVVGALPKALA 237 494  2833384 252 ------PP---PLAGTN------V-----MNIILVSAECAPWSKTGGLGDVAGSLPKALA 291 495  2129898 252 ------PP---PLAGTN------V-----MNIILVSAECAPWSKTGGLGDVAGSLPKALA 291 503  6467503 253            PLAGDN------V-----MNVILVAAECAPWSKTGGLGDVAGSLPKALA 290 496 15232051 291 ------KP--PPLAGAN------V-----MNVILVAAECAPFSKTGGLGDVAGALPKSLA 331 497  3192881 129 ------KP--PPLAGTN------V-----MNVILVCAECAPWSKTGGLGDVAGALPKALA 169 498  2833390 286 ------KP--PPLAGTN------V-----MNIILVASECAPWSKTGGLGDVAGALPKALA 326 499 14495348 248 ------DP--SASASVD------L-----INIILVAAECAPWSKTGGLGDVAGALPKALA 288 504  8708896 78            PLAGPN------V-----MNVVMVGAECAPWSKTGGLGDVMAALPKALV 115 525  2833387 1                                      EAAPYAKSGGLGDVCGSLPKALA 23 492 15237934 139                EV------V-----NNLVFVTSEAAPYSKTGGLGDVCGSLPIALA 172 484  5880466 137                 V------T-----RSIVFVTGEAAPYAKSGGLGDVCGSLPIALA 169 505  6690399 62                EV------V-----NNLVFVTSEAAPYSKTGGLGDVCGSLPIALA 95 485  9369334 137 ----------------V------T-----RSIVFVTGEAAPYAKSGGLGDVCGSLPIALA 169 486  6103327 137 ----------------V------T-----RSIVFVTGEAAPYAKSGGLGDVCGSLPIALA 169 487  7188796 126 ------ND--QPLA-KV------T-----RSIVFVTGEAAPYAKSGGLGDVCGSLPIALA 165 506  2829792 132                               NIIFVTAEAAPYSKTGGLGDVCGSLPMALA 161 507 12019656 140                               SIVFVTGEASPYAKSGGLGDVCGSLPVALA 169 493  7489712 110 VVASEQDS--EIVVGKEQARAKVT-----QSIVFVTGEASPYAKSGGLGDVCGSLPVALA 162 488  2833377 128 -------------QAKV------T-----RSVVEVTGEASPYAKSGGLGDVCGSLPIALA 163 489  1549232 128 -------------QAKV------T-----RSVVFVTGEASPYAKSGGLGDVCGSLPIALA 163 490  5295947 128 -------------QAKV------T-----RSVVFVTGEASPYAKSGGLGDVCGSLPIALA 163 500  6136121 70 ------GSPLGKIICGT------G-----MNLVFVLAEVGPWSKTGGLGDVVGGLPPAMA 112 508  5441242 80                         -----MNLIFVGAEVAPWSKTGGLGDVLGGLPSALA 110 509  2833388 82                         -----MNLIFVGAEVGPWSKTGGLGDVLGGLPPALA 112 510  3832512 79                 N------G-----MNLVFVGAEVGPWSKTGGLGDVLGGLPPALA 111 511 15223331 75        A--GKIVCEK------G-----MSVIFIGAEVGPWSKTGGLGDVLGGLPPALA 114 512  2833383 77                         -----MSLVEVGAEVCPWSKTGGLGDVLGGLPPVLA 107 513 15637079 67 ------EG--GMAAGTI------VCKQQGMNLVFVGCEVGPWCKTGGLGDVLGGLPPALA 112 514   267196 81                         -----MNLIFVGTEVGPWSKTGGLGDVLGGLPPALA 111 515   228210 81                         -----MNLIFVGTEVGPWSKTGGLGDVLGGLPPALA 111 516   602594 81                         -----MNLIFVGTEVGPWSKTGGLGDVLGGLPPALA 111 517   283338 182                         -----MNLVFVGCEEGPWCKTGGLGDVLGGLPPALA 112 518  1200328 578                         -----MTLIFVSAECGPWSKTGGLGDVVGGLPPALA 108 519  1562636 587                         -----MNLIFVGTEVAPWSKTGGLGDVLGGLPPALS 117 520   662428 173               GSG------G-----NNLVFVGAEMAPWSKTGGLGDVLGGLPAAMA 107 521   662428 773               GSG------G-----MNLVFVGAEMAPWSKTGGLGDVLGGLPPAMA 107 522   476058 473               GEG------G-----MNLVFVGAEMAPWSKTGGLGDVLGGLPPAMA 107 523  1813961 174            PIVCSA------G-----MTIIFIATECHPWCKTGGLGDVLGGLPPALA 111 524 17736918 3               GSG------G-----MNLVFVGAEMAPWSKTGGLGDVLGGLPPAMA 37 475 Maize SSIIa 272 RRGHRVMVVVPRY-------GD-------YVEAFDMGIRKYYKAAGQDLEVNYFHAFIDG 317 476  7489710 272 RRGHRVMVVVPRY-------GD-------YVEAFDMGIRKYYKAAGQDLEVNYFHAFIDG 317 477  8953573 338 KRGHRVMVVVPRY-------GD-------YEEAYDVGVRKYYKAAGQDMEVNYFHAYIDG 383 478  8953571 339 KRGHRVMVVVPRY-------GD-------YEEAYDVGVRKYYKAAGQDMEVNYFHAYIDG 384 479  5825480 339 KRGNRVMVVVPRY-------GD-------YEEAYDVGVRKYYKAAGQDMEVNYFHAYIDG 384 480  7529653 339 KRGHRVMVVVPRY-------GD-------YEEAYDVGVRKYYKAAGQDMEVNYFHAYIDG 384 482 16265834 350 RRGHRVMVVVPRY-------GD-------YAEAQDVGIRKYYKAAGQDLEVKYFHAFIDG 395 525  7489695 31 KRGHRVMVVVPRY-------GD-------YEEAYDVGVRKYYKAAGQDMEVNYFHAYIDG 76 491 15384987 177 RRGHRVMVVIPRY-------GE-------YAEAKDLGVRKRYRVAGQDSEVSYFHAFIDG 222 482 15028467 234 RRGERVMVVIPRY-------GE-------YAEAKDLGVRKRYRVAGQDSEVSYFHAFIDG 279 483  7489711 238 RRGHRVMVVIPRY-------GE-------YAEARDLGVRRRYKVAGQDSEVTYFHSYIDG 283 494  2833384 292 RRGHRVMIVAPRY-------GN-------YAEANDIGVRKRYKVAGQDMEVTYFHTYIDG 337 495  2129898 292 RRGHRVMIVAPHY-------GN-------YAEANDIGVRKRYKVAGQDMEVTYFHTYIDG 337 503  6467503 291 RRGNRVMVVAPRY-------GN-------YVEFQDTGVRKRYKVDGQDFEVSYFQAFIDG 336 496 15232051 332 RRGERVMVVVPRY-------AB-------YAEAKDLGVRKRYKVAGQDMEVMYFHAFIDG 377 497  3192881 170 RRGHRVMVVVPLY-------GN-------YAEPQHTGVRKMFKIDGQDMEXNYFHAYIDN 215 498  2833390 327 RRGHRVMVVAPRY-------DN-------YPEPQDSGVRKIYKVDGQDVDVTYFQALLMD 372 499 14495348 289 RRGHRVMVVVPMY-------KM-------YAEPQQLGEPRRYQVAGQDMEVIYYHAYIDG 334 504  8708896 116 RRGHRVMVVVPRY-------EN-------YDNAWETGIRKIYSVFNSNQEVGYFHAFVDG 161 525  2833387 24 ARGHRVMVVMPRYLNGSSD-KN-------YAKALYTAKHIKIPCFGGSEEVTFFHEYRDN 75 492 15237934 173 GRGHRVMVISPRYLNGTAALKN-------YARAKDLGIRVTVNCFGGSQEVSFYNEYRDG 225 484  5880466 170 ARGHRVMVVMPRYLMGSSD-KN-------YAKALYTGKHIKIPCFGGSHEVTFFHEYRDN 221 505  6690399 96 GRGNRVMVISPRYLNGTAADKN-------YARAKDLGIRVTVNCFGGSQEVSFYHEHRDG 148 485  9369334 170 ARGMRVMVVMPRYLNGSSD-KN-------YAKALYTGKEIKIPCFGGSHEVTFFHEYRDN 221 486  6103327 170 ARGHRVMVVMPRYLNGSSD-KN-------YAKALYTAKHIKIPCFGGSHEVTFFNEYRDN 221 487  7188796 166 ARGHRVMVVMPRYLNGTSD-KN-------YAKALYTGKHIKIPCFGGSHEVTFFEEYRDN 217 506  2829792 162 ARGNRVMVVSPRY-------LNGGPSDEKYANAVDLDVRATVHCFGDAQEVAFYHEYRAG 214 507 12019656 170 ARGNRVMVVMPRYLNGTSD-KN-------YANAFYTEKMIRIPCFGGEHEVTFFHEYRDN 221 493  7489712 163 ARGHRVMVVMPRYLNGTSD-KN-------YANAFYTEKHIRIPCFGGEHEVTFFHEYRDS 214 488  2833377 164 LRGHRVMVVMPRYMNGALN-KN-------FANAFYTEKHIKIPCFGGENEVTFFHEYRDS 215 489  1549232 164 LRGHRVMVVMPRYMNGALN-KN-------FANAFYTEKXIKIPCFGGEHEVTFFMEYRDS 215 490  5295947 164 LRGHRVMVVMPRYMNGALN-KN-------FANAFYTEKHIKIFCFGGEHEVTFFHEYRDS 215 500  6136121 113 GNGHRVMTVSPRY-------DQ-------YKDAWDTSVVVEIKVGDSIETVRFFHCYKRG 158 508  5441242 111 EHGERVMTVSPRY-------DQ-------YKDAWDTNVTVEVKVADRIETVRFFHCYKQG 156 509  2833388 113 ARGHRVMTVSPRY-------DQ-------YKDAWDTSVSVEIKIGDRIETVRFFHSYKRG 158 510  3832512 112 GMGHRVMTVSPRY-------DQ-------YKDAWDTGVSVEIKVGDRFETVRFFWCYKRG 157 511 15223331 115 ARGHRVMTVCPRY-------DQ-------YKDAWDTCVVVQIKVGDKVENVRFFHCYKRG 160 512  2833383 108 GNGHRVMTVSPRY-------DQ-------YKDAWDTNVLVEVKVGDKIETVRFFHCYKRG 153 513 15637079 113 ARGHRVMTVCPRY-------DQ-------YKDAWDTCVVVEIKIGDRIEPVRFFHSYKRG 158 514   267196 112 ARGHRVMTTSPRY-------DQ-------YKDAWDTSVAVEVKVGDSIEIVRFFHCYKRG 157 515   228210 112 ARGHRVNTISPRY-------DQ-------YKDAWDTSVAVEVKVGDSIEIVRFFHCYKRG 157 516   602594 112 ARGHRVMTISPRY-------DQ-------YKDTWDTSVAVEVKVGDSIEIVRFFHCYKRG 157 517  2833381 113 ARGHRVMTVCPRY-------DQ-------YKDAWETCVVVEPQVGDRIEPVRFFHSYKRG 158 518 12003285 109 ANRHRVMTVSPRY-------DQ-------YKDAWDTSVVVEIQVGDKVETVGFFHCYKRG 154 519 15626365 118 ANGHRVMTVTPRY-------DQ-------YKDAWDTNVTIEVKVGDRTEKVRFFHCFKRG 163 520  6624281 108 ANGHRVMVISPRY-------DQ-------YKDAWDTSVISEIKVVDRYERVRYFHCYKRG 153 521  6624287 108 ANGHRVMVISPRY-------DQ-------YKDAWDTSVVSEIKVALEYERVRTFHCYKRG 153 522  4760584 108 ANGNRVMVISPRY-------DQ-------YKDAWDTSVVSEIKVALKYERVRYFHCYKRG 153 523 18139611 112 AMGHRVMTIVPRY-------DQ-------YKDAWDTNVLVEVNIGDRTETVRFFHCYKRG 157 524 17736918 38 ANGHRVMVISPRY-------DQ-------YKDAWDTSVVSEIKVVDKYERVRYFHCYKRG 83 475 Maize SSIIa 318 VDFVFIDAPLFRH---R-----QDDIY----G---G----SR----QEIMK--------- 345 476  7489710 318 VDFVFIDAPLFRH---R-----QDDIY----G---G----SR----QEIMK--------- 345 477  8953573 384 VDFVFIDAPLFRH---R-----QEDIY----G---G----SR----QEIMK--------- 411 478  8953571 385 VDFVFIDAPIFRH---R-----QEDIY----G---G----SR----QEIMK--------- 412 479  5825480 385 VDFVFIDAPLFRH---R-----QEDIY----G---G----SR----QEIMK--------- 412 480  7529653 385 VDFVFIDAPLFRH---R-----QEDIY----G---G----SR----QEIMK--------- 412 481 16265834 396 VDFVFIDAPLFRH---R-----QDDIY----G---G----NR----QEIMK--------- 423 502  7489695 77 VDFVFIDAPLFRH---R-----QEDIY----G---G----SR----QEIMK--------- 104 491 15384987 223 VDFVFLEAPPFRH---R-----HNDIY----G---G----ER----FDVLK--------- 250 482 15028467 280 VDFVFLEAPPFRH---R-----HNDIY----G---G----ER----FDVLK--------- 307 483  7489711 284 VDFVFVEAPPFRH---R-----HNNIY----G---G----ER----LDILR--------- 311 494  2833384 338 VDIVFIDSPIFPN---L-----ESNIY----G---G----NR----LDILR--------- 365 495  2129898 338 VDIVFIDSPIFPN---L-----ESNIY----G---G----NR----LDILR--------- 365 503  6467503 337 VDFVFIDSPMFRH---I-----GNDIY----G---G----NR----MDILK--------- 364 496 15232051 378 VDFVFIDSPEFRH---L-----SNNIY----G---G----NR----LDILK--------- 405 497  3192881 216 VDFVFIDSPIFQH---R-----GNNIY----G---G----NR----VDILK--------- 243 498  2833390 373 CDFVFIHSHMFRH---I-----GNNIY----G---G----NR----VDILK--------- 400 499 14495348 335 VDFVFIDNPIFEH---V-----ENDIY----G---G----DR----TDILK--------- 362 504  8708896 162 VDYVFVDHPTFHG---R-----GKNIY----G---G----ER----QEILF--------- 189 488  2833387 76 VDWVFVDHPSY-H---R-----PGSLY----GDNFG----AF----GDNQF--------- 105 492 15237934 226 VDWVFVDHKSY-H---R-----PGNPY----G---D----SK----GAFGDNQF------ 255 484  5880466 222 VDWVFVDHPSY-H---R-----PGSLY----GDNFG----AF----GDNQF--------- 251 505  6690399 149 VDWVFVDHKSY-H---R-----PGNPY----G---D----SK----GAFGDNQF------ 178 485  9369334 222 VDWVFVDHPSY-H---R-----PGSLY----GDNFG----AF----GDNQF--------- 251 486  6103327 222 VDWVFVDHPSY-H---R-----PGSLY----GDNFG----AF----GDNQF--------- 251 487  7188796 218 VDWVFVDHPSY-H---R-----PGSLY----GDNFG----AF----GDNQF--------- 247 506  2829792 215 VDWVFVDNSSYCRPGTP-----YGDIY----GAF-G----DN----Q---F--------- 244 507 12019656 222 VDWVFVDHPSY-H---R-----PGNLY----GDKFG----AF----GDNQF--------- 251 493  7489712 215 VDWVFVDNPSY-H---R----RPGNLY----GDKFG----AF----GDNQF--------- 244 488  2833377 216 VDWVFVDHPSY-H---R-----PGNLY----GDNFG----AF----GDNQF--------- 245 489  1549232 216 VDWVFVDHPSY-H---R-----PGNLY----GDNFG----AF----GDNQF--------- 245 490  5295947 216 VDWVFVDHPSY-N---R-----PGNLY----GDNFG----AF----GDNQF--------- 245 500  6136121 159 VDRVFVDHPIFLE---KVWGKTKSKIY----G---P----NAGTDYQDNQL--------- 195 508  5441242 157 VDRVFVDHPCFLE---KVWGKTGSKLY----G---P----SAGVDYEDNQL--------- 193 509  2833388 159 VDRVFVDHPMFLE---KVWGKTGSKIY----G---PRAGLDY----QDNQL--------- 195 510  3832512 158 VDRVFVDHPLFLE---KVWGKTESKLY----G---P----KTGVDYKNQL---------- 194 511 15223331 161 VDRVFVDHPIFLA---KVGKTGSKIY----G---PITGVDY----NDNQL---------- 197 509  2833383 154 VDRVFVDHPLFLE---RVWGKTGSKLY----G---P----KTGIDYRDNQL--------- 190 513 15637079 159 VDRVFVDHPMFLE---KVWGKTGSMLY----G---P----KA----GKDYKDNQL----- 195 514   267196 158 VDRVFVDHPMFLE---K--------VW----G---K----TG----SKIYGPKAGLDYLD 191 515   228210 158 VDRVFVDHPMFLE---K--------VW----G---K----TG----SKIYGPKAGLDYLD 191 516   602594 158 VDRVFVDHPMFLE---K--------VW----G---K----TG----SKIYGPKAGLDYLD 191 517  2833381 159 VDRVFVDHPMFLE---KVWGKTGSMLY----G---P----KA----GKDYKDNQL----- 195 518 12003285 155 VDRVFVDHPLFLE---KVWGKTKSKVY----G---P----SAGVDYEDNQL--------- 191 519 15626365 164 VDRVFVDHPIFLE---KVWGKTGTKLY----G---P----AAGDDYQDNQL--------- 200 520  6624281 154 VDRVFVDHPCFLE---KVRGKTKEKIYGPDAG---T----DY----EDNQQ--------- 190 521  6624287 154 VDRVFVDHPCELE---KVRGKTKEKIY----GPDAG---TD----YEDNQL--------- 190 522  4760584 154 VDRVFVDHPCFLE---KVRGKTKEKIYGPDAG---T----DY----EDNQQ--------- 190 523 18139611 158 VDRVFVDHPMFLE---KVWGKTGPKLY----G---F----TT----GDDYRDNQL----- 194 524 17736918 84 VDRVFVDHPCFLE---KVRGKTKEKIYGPDAG---T----DY----EDNQQ--------- 120 475 (Maize SSIIa) 346 ---RMILFCKVAVEVPW-----HVPCGGV-----CYGDG----NLVFIANDWHTALLPVY 388 476  7489710 346 ---RMILFCKVAVEVPW-----HVPCGGV-----CYGDG----NLVFIANDWHTALLPVY 388 477  8953573 412 ---RMILFCKAAVEVPW-----HVFCGGV-----PYGDG----NLVFIANDWHTALLPVY 454 478  8953571 413 ---RMILFCKAAVEVFW-----HVPCGGV-----PYGDG----NLVFIANDWHTALLPVY 455 479  5825480 413 ---RMILFCKAAVEVPW-----HVPCGGV-----PYGDG----NLVFIANDWHTALLPVY 455 480  7529653 413 ---RMILFCKAAVEVPW-----HVPCGGV-----PYGDG----NLVFIANDWHTALLPVY 455 481 16265834 424 ---RMILFCKAAVEVPW-----HVPCGGV-----PYGDG----NLVFLANDWHTALLPVY 466 502  7489695 105 ---RMILFCKAAVEVPW-----HVPCGGV-----PYGDG----NLVFIANDWHTALLPVY 147 491 15384987 251 ---RMILFCKAAVEVPW-----FAPCGGS-----IYGDG----NLVFIANDWHTALLPVY 293 482 15028467 308 ---RMILFCKAAVEVPW-----FAPCGGS-----IYGDG----NLVFIANDWHTALLPVC 350 483  7489711 312 ---RMILFCKAAVEVPW-----YAPCGGT-----VYGDG----NLVFIANDWHTALLPVY 354 494  2833384 366 ---RMVLFCKAAVEVPW-----HVPCGGI-----CYGDG----NLVFIANDWHTALLPVY 408 495  2129898 366 ---RMVLFCKAAVEVPW-----HVPCGGI-----CYGDG----NLVFIANDWHTALLPVY 408 503  6467503 365 ---RMVLFCKAAVEVPW-----HVPCGGV-----CYGDG----NLAFIANDWHTALLPVY 407 492 15232051 406 ---RMVLFCKAAVEVPW-----YVPCGCV-----CYGDG----NLAFIANDWHTALLPVY 448 497  3192881 244 ---RMDLFCKAAIVVPW-----HVPCGGI-----CYGDG----NLVFIANDWNTALLPVY 286 498  2833390 401 ---RMVLFCKAAIEVPW-----HVPCGGV-----CYGDG----NLVFIANDWHTALLPAY 443 499 14495348 363 ---RMVLLCKAAIEVPW-----YVPCGGY-----CYGDG----NLVFLANDWHTALLPVY 405 504  8708896 190 ---RCALLCKAALEAVW-----HVPCGGI-----TYGDD----NLCFIANDWHTALLPVY 232 488  2833387 106 ---RYTLLCYAACEAFL-----ILELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 147 492 15237934 256 ---RFTLLCHAACEAPL-----VLFLGGF-----TYGEK----SL-FLVNDWHAGLVPIL 297 484  5880466 252 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 293 505  6690399 179 ---RFTLLCHAACEAPL-----VLPLGGF-----TYGEK----SL-FLVNDWHAGLVPIL 220 485  9369334 252 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 293 486  6103327 252 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 293 484  7188796 248 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----SCMFVVNDWHASLVPVL 289 506  2829792 245 ---RFTLLSHAACEAPL-----VLPLGGF-----TYGEK----CL-FLANDWHAPLVPLL 286 507 12019656 252 ---RYTLLCYAACEAPL-----VLELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 293 493  7489712 245 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----NCMFVVNDWHASLVPVL 286 488  2833377 246 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----KCMFVVNDWHASLVPVL 287 489  1549232 246 ---RYTLLCYAACEAPL-----ILELGGY-----IYGQ-----KCMFVVNDWHASLVPVL 287 490  5295947 246 ---RYTLLCYAACEAPL-----ILEEGGY-----IYGQ-----KCMFVVNDWHASLVPVL 287 500  6136121 196 ---RFSLLCQAALEAPR-----VLNLTSS-----KYFSGPYGEDVVFVANDWHTALLPCY 242 508  5441242 194 ---RYSLLCQAALEAPR-----VLNLNSN-----KYFSGPYGEDVIFVANDWHTALLPCY 240 509  2833388 196 ---RFSLLCLAALEAPR-----VLNLNSSKNFSGPYGE-----EVAFIANDWHTALLPCY 242 510  3832512 195 ---RFSLLCQAALEAPR-----VLNLNSN-----KHFSGPYGEDVVFVANDWHTALLPCY 241 511 15223331 198 ---RFSLLCQAALEAPQ-----VLNLNSS-----KYFSGPYGEDVVFVANDWHTALLPCY 244 512  2833383 191 ---RFSLLCQAALEAPR-----VLNLNSS-----KYFSGPYGEDVIFVANDWHSALIPCY 237 513 15637079 196 ---RFSLLCQAALEAPR-----VLNLNSS-----NYFSGPYGEDVVFVANDWHTALLPCY 242 514   267196 192 NELRFSLLCQAALEAPK-----VLNLNSS-----NYFSGPYGEDVLFIANDWHTALIPCY 241 515   228210 192 NELRFSLLCQAALEAPK-----VLNLNSS-----NYFSGPYGEDVLFIANDWHTALIPCY 241 516   602594 192 NELRFSLLCQAALEAPK-----VLNLNSS-----NYFSGPYGEDVLFIANDWHTALIPCY 241 517  2833381 196 ---RFSLLCQAALEAPR-----VLNLNSS-----KYFSGPYGEDVVFVANDWHTAWLPCY 242 518 12003285 192 ---RFSLLSLAALEAPP-----VLNLTSN-----KYFSGPYGEDVVFVANDWETAVLPCY 238 519 15626365 201 ---RFSIFCQAALEAAR-----VLNLKSN-----KYFSGPYGEDVIFVANDWHTALISCY 247 520  6624281 191 ---RFSLLCQAALEVPRILDLNNNPHFSG-----PYGE-----DVVFVCNDWHTGLLACY 237 521  6624287 191 ---RFSLLCQAALEAPR-----ILDLNNN-----PYFSGPYGEDVVFVCNDWHTGLLACY 237 522  4760584 191 ---RFSLLCQAALEVPR-----ILNLDNN-----PYFSGPYGEDVVFVCNDWHTGLLACY 237 523 18139611 195 ---RFCLLCLAALEAPR-----VLNLNNS-----EYFSGPYGENVVFVANDWHTGVLPCY 241 524 17736918 121 ---RFSLLCQAALEVPR-----ILNLDNN-----PYFSGPYGEDVVFVCNDWHTGLLACY 167 475 Maize SSIIa 389 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 441 476  7489710 389 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 441 477  8953573 455 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 507 478  8953571 456 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 508 479  5825480 456 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 508 480  7529653 456 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 508 481 16265834 467 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 519 502  7489695 148 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 200 491 15384987 294 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 346 482 15028467 351 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 403 483  7489711 355 LKAYYRDHGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQHFELYD----PV--- 407 494  2833384 409 LKAYYRDHGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLDLFKMYD----PV--- 461 495  2129898 409 LKAYYRDHGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLDLFKMYD----PV--- 461 503  6467503 408 LKAYYRDNGLMQYTRSVLVIHNIAHQGRGPSGDFSYVGLPEHYIDLFKLHD----PI--- 460 492 15232051 449 LKAYYRDHGIMKYTRSVLVIHNIAHQGRGPVDDFSYVDLPSHYLDSFKLYD----PV--- 501 497  3192881 287 LKAYFRDNGVMKFTRSVLVIHNIAHQGRGPMDDFSIVDLPAQUADLFKLYD----PV--- 339 498  2833390 444 LKAYYRDNGIMNYTRSVLVIHNIAHQGRGPLEDFSYVDLPPHYMDPFKLYD----PV--- 496 499 14495348 406 LKAYYHDNGFMIYARSVLVIHNIAHQGRGPLDDFSYLDLPVDYMDLFKLYD----PF--- 458 504  8708896 233 LQAHYRDYGEMTYARCAFVIHNMAHQGRGPFVESEHLELNEEYRERFRLYD----PI--- 285 488  2833387 148 LAAKYRPYGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 203 492 15237934 298 LAAKYRPYGVYKDARSILIIHNLAHQGVEPAATYTNLGLPS------EWYG----AV--- 344 484  5880466 294 LAAKYRPYGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 349 505  6690399 221 LAAKYRPYGVYKDARSILIIHNLAHQGVEPAATYTNLGLPS------EWYG----AV--- 267 485  9369334 294 LAAKYRPYGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 349 486  6103327 294 LAAKYRPYGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 349 487  7188796 290 LAAKYRPYGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 345 506  2829792 287 LAAKYRPYGVYKDARSIVAIHNIAHQGVEPAVTYNNLGLPPQWYGAVEWIF----PTWAR 342 526  7484400 4                          RGRGPFVESEHLELNEEYRERFRLYD----PI--- 31 507 12019656 294 LAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 349 493  7489712 287 LAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 342 488  2833377 288 LAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 343 489  1549232 288 LAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 343 490  5295947 288 LAAKYRPYGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVF----PEWAR 343 500  6136121 243 LKSMYQSKGMYLHAKVAFCIHNIAYQGRFGSSDFCLLNLPDQFKSSFDFFDGYEKPV--- 299 508  5441242 241 LKSMYQTRGVYRNTKVAFCIHNISYQGRHPFEDFPLLNLPNEYRSAFDFTDGHLKPV--- 297 509  2833388 243 LKAIYQPMGIYKHAKVAFCIHNIAYQGRFAFSDFFRLNLPDKFKSSFDFIDGYEKPV--- 299 510  3832512 242 LKSLYKSKGIYKSAKVAFCIHNIAYQGPYAFSDLSLLNLPNEFRSSFDFIDGYDKPV--- 298 511 15223331 245 LKSMYQSRGVYMNAKVVFCIHNIAYQGRFAFDDYSLLNLPISFKSSFDFMDGYEKPV--- 301 512  2833383 238 LKSMYKSRGLYKNAKVAFCIHNIAYQGRNAFSDFSLLNLPDEFRSSFDFIDGYNKPC--- 294 513 15637079 243 LKTMYQSRGIYNNAKVAFCIWNIAYQGRFAFSDFSLLNLPDEYKGSFDFIDGYDKPV--- 299 514   267196 242 LKSMYQSRGIYLNAKVAFCINNIAYQGRFSFSDFPLLNLPDEFRGSFDFIDGYEKPV--- 298 515   228210 242 LKSMYQSRGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRGSFDFIDGYEKPV--- 298 516   602594 242 LKSMYQSRGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRGSFDFIDGYEKPV--- 298 517  2833381 243 LKTMYQSRGIYMNAKVAFCIHNIAYQGRFAFSDFSLLNLPDEYKGSFDFIDGYDKPV--- 299 518 12003285 239 LKTIYQPKGIYTNAKVVLCIHNIAYQGRFAFSDFYKLNLPDQLKSSFDFMDGYEKPV--- 295 519 15626365 248 MKSMYQSIGIFRNAKVVFCIHNIAYQGRFAFTDYSLLNLPDQFKSSFDFLDQWIKPI--- 304 520  6624281 238 LKSNYQSNGIYRTAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSFDFIDGYDKPV--- 294 521  6624287 238 LKSNYQSNGIYMTAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSFDFIDGYDKPV--- 294 522  4760584 238 LKSNYQSNGIYRAAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSFDFIDGYDKPV--- 294 523 18139611 242 LKSIYQAKGMYThAKVAFCIHNIAYQGRFAREDFELLNLPDSELPSFDFIDGHFKPV--- 298 524 17736918 168 LKSNYQSNGIYRAAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSFDFIDGYDKPV--- 224

[0394] TABLE XXI Maize soluble starch synthase IIa (SSIIa) “LINKR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)               sequence               end # 527 MaizeSSIIa 442 ----G--------------GEHANIFAAGLKMADRVVTVSRGYLWE-L-KT-VEG-GWG 478 528  7489710 442 ----G--------------GEHANIFAAGLKMADRVVTVSRGYLWE-L-KT-VEG-GWG 478 529  8953573 508 ----G--------------GEHANYFAAGLKMADQVVTVSPGYLWE-L-KT-VEG-GWG 544 530  8953571 509 ----G--------------GEHANYFAAGLKMADQVVVVSPGYLWE-L-KT-VEG-GWG 545 531  5825480 509 ----G--------------GEHANYFAAGLKMADQVVVVSPGYLWE-L-KT-VEG-GWG 545 532  7529653 509 ----G--------------GEHANYFAAGLKMADQVVVVSPGYLWE-L-KT-VEG-GWG 545 533 16265834 520 ----G--------------GEHANIFGAGLKMADRVVTVSPGYLWE-L-KT-TEG-GWG 556 534  7489695 201 ----G--------------GEHANYFAAGLKMADQVVTVSPGYLWE-L-KT-VEG-GWG 237 535 15384987 347 ----G--------------GEHSNVFAAGLKMADRAVTVSHGYLWE-I-KT-MDG-GWG 383 536 15028467 404 ----G--------------GEHSNVFAAGLKMADRAVTVSHGYLWE-I-KT-MDG-GWG 440 537  7489711 408 ----G--------------GDHSNVFAAGLKTALRVVTVSNGYMWE-L-KT-SEG-GWG 444 538  2833384 462 ----G--------------GEHFNIFAAGLKTADRIVTVSHGYAWE-L-KT-SEG-GWG 498 539  2129898 462 ----G--------------GEHFNIFAAGLKTALRIVTVSHGYAWE-L-KT-SEG-GWG 498 540  6467503 461 ----G--------------GDHFNIFAPGLKVADRVVTVSHGYAWE-L-KT-SEG-GWG 497 541 15232051 502 ----G--------------GEHFNIFAAGLKAADRVLTVSHGYSWE-V-KT-LEG-GWG 538 542  3192881 340 ----G--------------GDHFNIFAAGLKTADRVVTVSHGYAWE-L-KT-SEG-GWG 376 543  2833390 497 ----G--------------GEHFNIFAAGLKTADRVVTVSHGYSWE-L-KT-SQG-GWG 533 544 14495348 459 ----G--------------GDHLNIFAAGIKAADRLLTVSHGYAWE-L-KT-AEG-GWG 495 545  8708896 286 ----G--------------GEHMNVMKAGLECAHRLVAVSKCYAWE-C-QT-VEG-GWG 322 546  2833387 204 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 245 547 15237934 345 -----GWVFPTWARTHALDTGEAVNLKGAIVTSDRIITVSQGYAWE-I-TT-VEG-GYG 395 548  5880466 350 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 391 549  6690399 268 -----GWVFPTWARTHALDTGEAVNLKGAIVTSDRIITVSQGYAWE-I-TT-VEG-GYG 318 550  9369334 350 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGY8WE-V-TT-AEG-GQG 391 551  6103327 350 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 391 552  7188796 346 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 387 553  2829792 343 AHALDT-------------GETVNVLKGAIAVADRILTVSQGYSWE-I-TT-PEG-GYG 384 554  7484400 32 ----G--------------GEHMNVMKAGLECAHRLVAVSKCYAWE-C-QT-VEG-GWG 68 555 12019656 350 RHALDK-------------GEAVNFLKGAVVTAHPLVTVSKGYSWE-V-TT-AEG-GQG 391 556  7489712 343 RHALDK-------------GEAVNFLKGAVVTADRIVTVSKGYSWE-V-TT-AEG-GQG 384 557  2833377 344 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 385 558  1549232 344 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 385 559  5295947 344 RHALDK-------------GEAVNFLKGAVVTADRIVTVSQGYSWE-V-TT-AEG-GQG 385 560  6136121 300 -----K-------------GRKINWMKAGILESDRVVTVSPYYAME-L-VSGAEK-GVE 337 561  5441242 298 -----R-------------GRKINWMKAAILESDLVLTVSPYYAKE-L-VS-GEDRGVE 335 562  2833388 300 -----K-------------GRKINWMKAGILESDRVLTVSPYYAQEVI-SG-VER-GVE 337 563  3832512 299 -----K-------------GRKINWMKAGVLESDRVFTVSPYYAKE-L-VS-GEDRGVE 336 564 15223331 302 -----K-------------GRKINWMKAAILEAHRVLTVSPYYAQE-L-ISGVDR-GVE 339 565  2833383 295 -----E-------------GKKINWMKAGILESDQVFTVSPHYAKE-L-IS-GEDRGVE 332 566 15637079 300 -----K-------------GRKINWMKAGIREADRVFTVSPNYAKE-L-VSCVSK-GVE 337 567   267196 299 -----K-------------GRKINWMKAGILESHRVVTVSPYYAQE-LVSA-VDK-GVE 336 568   228210 299 -----K-------------GRKINWMKAGILESHRVVTVSPYYAQE-LVSA-VDK-GVE 336 569   602594 299 -----K-------------GRKINWMKAGILESHRVVTVSPYYAQE-L-VSAVDK-GVE 336 570  2833381 300 -----K-------------GRKINWMKAGIREADRVFTVSPNYAKE-L-VSCVSK-GVE 337 571 12003285 296 -----K-------------GRKINWMKAGIIESDRVLTVSPYYAKE-L-VSGPDK-GVE 333 572 15626365 305 -----V-------------GRKINWMkAGIIESHRVLTVSPYYAQE-L-VSGPDK-GVE 342 573  6624281 295 -----E-------------GRKINWMKAGILQADKVLTVSPYYAEE-L-IS-GEARGCG 332 574  6624287 295 -----E-------------GRKINWMKAGILQADKVLTVSPYYAEE-L-IS-GEARGCE 332 575  4760584 295 -----E-------------GRKINWMKAGILQADKVLTVSPYYAEE-L-IS-GEARGCE 332 576 18139611 299 -----V-------------GRKINWMKAGITECDLVMTVSPHYVKE-L-ASGPDK-GVE 336 577 17736918 225 -----E-------------GRKINWMKAGILQADKVLTVSPYYAEE-L-IS-GETRGCE 262 527 Maize SSIIa 479 LHDIIRSNDWKINGIVNGIDHQEWNPKVDVHL-RSDGYTN--YSLETLDAGKRQCKAALQ 535 528  7489710 479 LHDIIRSNDWKINGIVNGIDHQEWNPKVDVHL-RSDGYTN--YSLETLDAGKRQCKAALQ 535 529  8953573 545 LHDIIRQNDWKTRGIVNGIDNMEWNPEVDVHL-KSDGYTN--FSLGTLDSGKRQCKEALQ 601 530  8953571 546 LHDIIRQNDWKTRGIVNGIDNMEWNPEVDVHL-QSDGYTN--FSLSTLDSGKRQCKEALQ 602 531  5825480 546 LHDIIRQNDWKTRGIVNGIDNMEWNPEVDVHL-KSDGYTN--FSLGTLDSGKRQCKEALQ 602 532  7529653 546 LHDIIRQNDWKTRGIVNGIDNMEWNPEVDVHL-KSDGYTN--FSLGTLDSGKRQCKEALQ 602 533 16265834 557 LHDIIRENDWKMNGIVNGIDYREWNPEVDVHL-QSDGYAN--YTVASLDSSKPRCKAALQ 613 534  7489695 238 LHDIIRQNDWKTRGIVNGIDNMEWNPEVDVHL-KSDGYTN--FSLGTLDSGKRQCKEALQ 294 535 15384987 384 LHEIINHNDWKLQGIVNGIDMAEWNPEVDEHL-QSDGYAN--YTFETLDTGKKQCKEALQ 440 536 15028467 441 LHEIINHNDWKLQGIVNGIDMAEWNPEVDEHL-QSDGYAN--YTFETLDTGKKQCKEALQ 497 537  7489711 445 LHDIINQNDWKLQGIVNGIDMSEWNPAVDVHL-HSDDYTN--YTFETLDTGKRQCKAALQ 501 538  2833384 499 LHNIINESDWKFRGIVNGVDTKDWNPQFDAYL-TSDGYTN--YNLKTLQTGKRQCKAALQ 555 539  2129898 499 LHNIINESDWKFRGIVNGVDTKDWNPQFDAYL-TSDGYTN--YNLKTLQTGKRQCKAALQ 555 540  6467503 498 LHNIINENHWKLQGIVNGIDAKEWNPQFDIQL-TSDGYTN--YSLETLDTGKPQCKTALQ 554 541 15232051 539 LHNIINENDWKFRGIVNGIDTQEWNPEFDTYL-HSDDYTN--YSLENLHIGKPQCKAALQ 595 542  3192881 377 LNGIRNENEWKLQGIVNGIDIEEWNPQLDVYL-KSDGYAN--YSLDTLQTGKPQCKAALQ 433 543  2833390 534 LHQIINENDWKLQGIVNGIDTKEWNPELDVHLPRSDGYMN--YSLDTLQTGKPQCKAALQ 591 544 14495348 496 LHGIINESDWKFQGIVNGIDTTDWNPRCDIHL-KSDGYTN--YSLETVQAGKQQCKAALQ 552 545  8708896 323 LHEVIKVNNWKLRGIVNGIDYKEWNPICDEFL-TTDGYAH--YDVDTLAEGKAKCKAALQ 379 546  2833387 246 LNELLSSRKSVLNGIVNGIDINDWNPTTDKCL-PH----H--YSVDDL-SGKAKCKAELQ 297 547 15237934 396 LQDLLSSRKSVINGITNGINVDEWNFSTDEHI-P----FH--YSADDV-SEKIKCKNALQ 447 548  5880466 392 LNELLSSRKSVLNGIVNGIDINDWNPTTDKCL-PH----H--YSVDDL-SGKAKCKAELQ 443 549  6690399 319 LQDLLSSRKSVINGITNGINVDEWNPSTDEHI-P----FH--YSADDV-SEKIKCKAELQ 370 550  9369334 392 LNELLSSRKSVLNGIVNGIDINDWNPTTDKCL-PH----H--YSVDDL-SGKAKCKAELQ 443 551  6103327 392 LNELLSSRKSVLNGIVNGIDINDWNPTTDKCL-PH----H--YSVDDL-SGKAKCKAELQ 443 552  7188796 388 LNELLSSRKSVLNGIVNGIDINDWNPTTDKCL-PH----H--YSVDDL-SGKAKCKAELQ 439 553  2829792 385 LHELLSSRQSVLNGITNGIDVNDWNPSTDEHI-AS----H--YSINDL-SGKVQCKTDLQ 436 554  7484400 69 LHEVIKVNNWKLRGIVNGIDYKEWNPICDEFL-TTDGYAH--YDVDTLAEGKAKCKAALQ 125 555 12019656 392 LNELLSSRKSVLNGIVNGIDINDWNPATDKCI-P----CH--YSVDDL-SGKAKCKGALQ 443 556  7489712 385 LNELLSSRKSVLNGIVNGIDINDWNPATDKCI-P----CH--YSVDDL-SGKAKCKGALQ 436 557  2833377 386 LNELLSSRKSVLNGIVNGIDINDWNPSTDKFL-P----YH--YSVDDL-SGKAKCKAELQ 437 558  1549232 386 LNELLSSRKSVLNGIVNGIDINDWNPSTDKFL-P----YH--YSVDDL-SGKAKCKAELQ 437 559  5295947 386 LNELLSSRKSVLNGIVNGIDINDWNPSTDKFL-P----YH--YSVDDL-SGKAKCKAELQ 437 560  6136121 338 LDNVIAKT--SITGIVNGMDTQEWNPATDKHI-D----TN--YDITTVMDAKPLLKEALQ 388 561  5441242 336 LDNIIRKTG--VAGIVNGMDIREWSPKTDKFI-D----IH--FDTTSVKEAKFLLKEALQ 386 562  2833388 338 LDNFIRKTG--IAGIIHGMDVQEWNPVTDKYI-D----IH--YDATTVMDAKPLLKEALQ 388 563  3832512 337 LDNIIRS--IGITGIVNGMDNREWSPQTDRYI-D----VH--YDASTVTEAKAILKEALQ 387 564 15223331 340 LHKYLRMK--TVSGIINGMDVQEWNPSTDKYI-D----IK--YDITTVTDAKPLIKEALQ 390 565  2833383 333 LDNIIRSTG--IIGIVNGMDNREWSPQTDRYI-D----VH--YNETTVTEAKPLLKGTLQ 383 566 15637079 338 LDNHIR--DCGITGICNGMLTQEWNPATDKYL-A----VK--YDITTVMQAKPLLKEALQ 388 567   267196 337 LDSVLRKT--CITGIVNGMDTQEWNPA-------TDKYTDVKYDITTVMDAKPLLKEALQ 387 568   228210 337 LDSVLRKT--CITGIVNGMDTQEWNPA-------TDKYTDVKYDITTVMDAKPLLKEALQ 387 569   602594 337 LDSVLRKT--CITGIVNGMDTQEWNPA-------TDKYTDVKYDITTVMDAKPLLKEALQ 387 570  2833381 338 LDNHIR--DCGITGICNGMDTQEWNPATDKYL-A----VK--YDITTVMQAKPLLKEALQ 388 571 12003285 334 LDNILRK--CTVTGIVNGMDTQEWNPATDKYI-DN----H--YDITTVMDGKPLLKEALQ 384 572 15626365 343 LDNILRRVG--VTGIVNGMDVQEWNPSTDKYI-S----IK--YDASTVLEGKALLKEELQ 393 573  6624281 333 LDNIMRLTG--ITGIVNGMDVSEWDPIKDKFL-T----VN--YDVTTALEGKALNKEALQ 383 574  6624287 333 LDNIMRLTG--ITGIVNGMLVSEWDPTKDKFL-A----VN--YDVTTALEGKALNKEALQ 383 575  4760584 333 LDNIMRLTG--ITGIVNGMDVSEWDPTKDKFL-A----VN--YDITTALEGKALNKEALQ 383 576 18139611 337 LDGILRTKPLE-TGIVNGMDVYEWNPATDQYI-S----VK--YDATTVTEARALNKEMLQ 388 577 17736918 263 LDNIMRLTG--ITGIVNGNDVSEWDPTKDKFL-A----VN--YDITTALEGKALNKEALQ 313

[0395] TABLE XXII Maize soluble starch synthase IIa (SSIIa) “GLYTR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                Sequence                end # 578 MaizeSSIIa 536 RELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWI-AG-QDVQLVMLGTGRADLERMLQ 593 579  7489710 536 RELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWI-AG-QDVQLVMLGTGRADLERMLQ 593 580  8953571 602 RELGLQVRGDVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGPHDLEGMLR 659 581  8953571 603 RELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLR 660 582  5825480 603 RELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLR 660 583  7529653 603 RELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLQ 660 584 16265834 614 RELGLERVDDVPLIGFIGRLDGQKGVDIIGDAMPWI-AG-QDVQLVLLGSGRRDLEVMLQ 671 585  7489695 295 RELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLQ 352 586 15384987 441 RQLGLQVRDDVPLIGFIGRLDHQKGVDIIGDAMPWI-AG-QDVQVVMLGTGRPDLEEMLR 498 587 15028467 498 RQLGLQVRDDVPLIGFIGRLDHQKGVDIIGDAMPWI-AG-QDVQVVMLGTGRPDLEEMLR 555 588  7489711 502 RQLGLQVRDDVPLIGFIGRLDHQKGVDIIADAIHWI-AG-QDVQLVMLGTGRADLEDMLR 559 589  2833384 556 RELGLPVREDVPIISFIGRLDHQKGVDLIAEAIPWM-MS-HDVQLVMLGTGRADLEQMLK 613 590  2129898 556 RELGLPVREDVPIISFIGRLDHQKGVDLIAEAIPWM-MS-HDVQLVMLGTGRADLEQMLK 613 591  6467503 555 NELRFAIPPDVPVIGFIGRLDYQKGVDLIAEAIPWM-VG-QDVQLVMLGTGRQDLEEMLR 612 592 15232051 596 KELGLPVRPDVPLIGFIGRLDHQKGVDLIAEAVPWM-MS-QDVQLVMLGTGRPDLEEVLR 653 593  3192881 434 KEMNLPVRDDVPLIGFIGRLDHQKGVDLIAEAIPWM-MG-QDVQLVMLGTGRPDLEQMLK 491 594  2833390 592 KELGLPVRDDVPLIGFIGRLDPQKGVDLIAEAVPWM-MG-QDVQLVMLGTGRPDLEQMLR 649 595 14495348 553 KELGLPVRGDVPVIAFIGRLDHQKGVDLIAEAMPWI-AG-QDVQLIMLGTGRQDLEDTLR 610 596  8708896 380 KELGLPVDPDAPMLGFIGRLDYQKGVDLIRDNYDYI-MG-EKCQLVMLGSGRQDLEDALR 437 597  2833387 298 KELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMR 355 598 15237934 448 KELGLPIRPECPMIGFIGRLDYQKGIDLIQTAGPDL-MV-DDIQFVMLGSGDPKYESWMR 505 599  5880466 444 KELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMR 501 600  6690399 371 KELGLPIRPECPMIGFIGRLDYQKGIDLIQTAGPDL-MV-DDIQFVMLGSGDPKYESWMR 428 601  9369334 444 KELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMR 501 602  6103327 444 KELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMR 501 603  7188796 440 RELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPDL-MR-EDVQFVMLGSGDPVFEGWMR 497 604  2829792 437 KELGLPIRPDCPLIGFIGRLDYQKGVDIILSAIPEL-MQ-NDVQVVMLGSGEKQYEDWMR 494 605  7484400 126 KELGLPVDPDAPMLGFIGRLDYQKGVDLIRDNYDYI-MG-EKCQLVMLGSGRQDLEDALR 183 606 12019656 444 KELGLPIRPEVPLIGFIGRLDYQKGIDLIQLIIPHL-MR-DDVQFVMLGSGDPELEDWMR 501 607  7489712 437 KELGLPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDL-MR-EDVQFVMLGSGDPELEDWMR 494 608  2833377 438 KELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMR 495 609  1549232 438 KELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMR 495 610  5295947 438 KELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMR 495 611  6136121 389 AAVGLPVDKNIPVIGFIGRLEEQKGSDILVAAISKF-VG-LDVQIIILGTGKKKFEQQIQ 446 612  5441242 387 AEVGLPVNRDIPLIGFIGRLEEQKGSDILVEAIPKF-ID-QNVQIIILGTGKKSMEKQIE 444 613  2833388 389 AEVGLPVDRNVPLIGFIGRLEEQKGSDIFVAAISQL-VE-HNVQIVILGTGKKKFEKQIE 446 614  3832512 388 AEVGLPVDRNIPVIGFIGRLEEQKGSDILVESIPKF-ID-QNVQIIVLGTGKKIMEKQIE 445 615 15223331 391 AAVGLPVDRDVPVIGFIGRLEEQKGSDILVEAISKF-MG-LNVQMVILGTGKKKMEAQIL 448 616  2833383 384 AEIGLPVDSSIPLIGFIGRLEEQKGSDILVEAIAKF-AD-ENVQIVVLGTGKKIMEKQIE 441 617 15637079 389 AAVGLPVDRNIFLIGFIGRLEEQKGSDILYAAISKF-IS-MDVQILILGTGKKKFEQQIE 446 618   297196 388 AAVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIE 445 619   228210 388 AAVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIE 445 620   602594 388 AAVGLPVDKKVPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIE 445 621  2833381 389 AAVGLPVDRNIPLIGFIGRLEEQKGSDILYAAISKF-IS-MDVQILILGTGKKKFEQQIE 446 622 12003285 385 AEVGLPVDP VPLVGFIGRLEEQKGSDILVAALHKF-IE-MDVQVVILGTGKKEFEKQIE 442 623 15626365 394 AEVGLPVDKNVPLIAFIGRLEEQKGSDILVEAIPQF-IK-ENVQIVALGTGKKEMEKQLQ 451 624  6624281 384 AEVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEI-VKEEDVQIVLLGTGKKKFERLLK 442 625  6624287 384 AEVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIVLLGTGKKKFERLLK 442 626  4760584 384 AEVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIVLLGTGKKKFERLLK 442 627 18139611 389 AEVGLPVDSSIPLIVFVGRLEEQKGSDILIAAIPEF-VE-GNVQIIVLGTGKKKMEEELI 446 628 17736918 314 AEVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIVLLGTGKKKFERLLK 372 578 MaizeSSIIa 594 HLEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVG 653 579  7489710 594 HLEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVG 653 580  8953571 660 HFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 719 581  8953571 661 HFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 720 582  5825480 661 HFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 720 583  7529653 661 HFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 720 584 16265834 672 RFEAQHNSKVRGWVGFSVKMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVG 731 585  7489695 353 HFEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 412 586 15384987 499 RFESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 558 587 15028467 556 RFESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYSTVPVVHAVG 615 588  7489711 560 RFESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVG 619 589  2833384 614 EFEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVG 673 590  2129898 614 EFEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVG 673 591  6467503 613 QFENQHRDKVRGWVGFSVKTAHRITAGADILLMPSRFEPCGLNQLYAMMYGTIPVVHAVG 672 592 15232051 654 QMEHQYRDKARGWVGFSVKTAHRITAGADILLMPSRFEPCGLNQLYAMNYGTIPVVHAVG 713 593  3192881 492 QIEGQYGDKVRGWVGFSVKTAHRITAGADILLMPSRFEPCGLNQLYAMSYGTVPVVHAVG 551 594  2833390 650 QFECQHNDKIRGWVGFSVKTSHRITAGADILLMPSRFEPCALNQLYAMKYGTIPVVHAVG 709 595 14495348 611 RLESQHYDRVRGWVGFSIRLAHRMTAGADILLMPSRFEPCGLNQLYAMMYGTVPVVHAVG 670 596  8708896 438 DMENRNKNQCRGWVGFSNKMAHRITAAADILLMPSRFEPCGLNQLYAMAYGTVPIVHSVG 497 597  2833387 356 STESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 415 598 15237934 506 SMEETYRDKFRGWVGFNVPISHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPVVHGTG 565 599  5880466 502 STESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 561 600  6690399 429 SMEETYRDKFRGWVGFNVPISHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPVVHGTG 488 601  9369334 502 STESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 561 602  6103327 502 STESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 561 603  7188796 498 STESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 557 604  2829792 495 HTENLFKDKFRAWVGFNVPVSHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPIVHSTG 554 605  7484400 184 DMENRNKNQCRGWVGFSNKMAHRITAAADILLMPSRFEPCGLNQLYAMAYGTVPIVHSVG 243 606 12019656 502 STESDFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATG 561 607  7489712 495 STESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATG 554 608  2833377 496 STESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 555 609  1549232 496 STESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 555 610  5295947 496 STESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTG 555 611  6136121 447 ELEVLYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTIPICASTG 506 612  5441242 445 QLEEIYPEKARGIAKFDGPLAHKIIAGSDFIMIPSRFEPCGLVQLHSMPYGTVPIVSSTG 504 613  2833388 447 HLEVLYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPIVASTG 506 614  3832512 446 QLEVTYPGKAIGVAKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTG 505 615 15223331 449 ELEEKFPGKAVGVAKFNVPLAHMITAGADFIIVPSRFEPCGLIQLHAMRYGTVPIVASTG 508 616  2833383 442 VLEEKYPGKAIGITKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTG 501 617 15637079 447 QLEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHAMRYGTPCICASTG 506 618   297196 446 QLEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTG 505 619   228210 446 QLEVLYPGKVKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTG 505 620   602594 446 QLEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTG 505 621  2833381 447 QLEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHAMRYGTPCICASTG 506 622 12003285 443 QLEELYPGKAVGVAKFNVPLAHKITAGADFMLVPSRFEPCGLIQLHAMRYGTIPICASTG 502 623 15626365 452 QLEISYPDKARGVAKFNVPLAHMMIAGADFILIPSRFEPCGLIQLQAMRYGTVPIVASTG 511 624  6624281 443 SVEEKFPTKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTG 502 625  6624287 443 SVEEKFPNKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTG 502 626  4760584 443 SIEEKFPSKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTG 502 627 18139611 447 LLEVKYPNTARGLAKFNVPLAHMMFAGADFIIVPSRFEPCGLIQLQGMRYGVVPICSSTG 506 628 17736918 373 SIEEKFPSKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTG 432 578 MaizeSSIIa 654 GLRDTV---------AP-FDPF----GDAGL----G---W--------TFDR---AEANK 681 579  7489710 654 GLRDTV---------AP-FDPF----GDAGL----G---W--------TFDR---AEANK 681 580  8953571 720 GLRDTV---------PP-FDPF----NHSGL----G---W--------TFDR---AEAQK 747 581  8953571 721 GLRDTV---------PP-FDPE----NHSGL----G---W--------TFDR---AEAHK 748 582  5825480 721 GVRDTV---------PP-FDPF----NHSGL----G---W--------TFDR---AEAHK 748 583  7529653 721 GLRDTV---------PP-FDPF----NHSGL----G---W--------TFDR---AEAHK 748 584 16265834 732 GLRDTM---------SA-FDPF----EDTGL----G---W--------TFDR---AEPHK 759 585  7489695 413 GLRDTV---------PP-FDPF----NHSGL----G---W--------TFDR---AEAHK 440 586 15384987 559 GLRDTV---------AP-FDPF----ADTGL----G---W--------TFDR---AEANR 586 587 15028467 616 GLRDTV---------AP-FDPF----ADTGL----G---W--------TFDR---AEANR 643 588  7489711 620 GLRDTV---------AP-FDPF----NDTGL----G---W--------TFDR---AEANR 647 589  2833384 674 GLRDTV---------QP-FNPF----DESGV----G---W--------TFDR---AEANK 701 590  2129898 674 GLRDTV---------QP-FNPF----DESGV----G---W--------TFDR---AEANK 701 591  6467503 673 GLRDTV---------QP-FDPF----NESGL----G---W--------TFDS---AESHK 700 592 15232051 714 GLRDTV---------QQ-FDPY----SETGL----G---W--------TFDS---AEAGK 741 593  3192881 552 GLRDTV---------QP-FDPF----NESGY----G---W--------TFGR---ARANQ 579 594  2833390 710 GLRDTV---------QP-FDPL----MSQDW----G---G--------PSDR---AEASQ 737 595 14495348 671 GLRDTV---------EH-YNPY----EESGL----G---W--------TFEK---AEANR 698 596  8708896 498 GLRDTV---------KQ-YSPF----ENVGT----G---W--------VFER---AEANK 525 597  2833387 416 GLRDTV---------ET-FNPFGAK-GEEGT----G---W--------AFSP---LTVDK 446 598 15237934 566 GLRDTV---------EN-FNPYAEGGAGTGT----G---W--------VFTP---LSKDS 597 599  5880466 562 GLRDTV---------ET-FNPFGAK-GEEGT----G---W--------AFSP---LTVDK 592 600  6690399 489 GLRDTV---------EN-FNFYAEGGAGAGT----c---W--------VFTP---LSKDS 520 601  9369334 562 GLRDTV---------ET-FNPFGAK-GEEGT----G---W--------AFSP---LTVDK 592 602  6103327 562 GLRDTV---------ET-FNPFGAK-GEEGT----G---W--------AFSP---LTVDK 592 603  7188796 558 GLRDTV---------ET-FNPFGAK-GEEGT----G---W--------AFSP---LTVEK 588 604  2829792 555 GLRDTV---------KD-FNPY----AQEGIGEGTG---W--------TFSP---LTSEK 586 605  7484400 244 GLRDTV---------KQ-YSPF----ENVGT----G---W--------VFER---AEANK 271 606 12019656 562 GLRDTV---------EN-FNPFGEN-GEQGT----G---W--------AFAP---LTTEN 592 607  7489712 555 GLRDTV---------EN-FNPFGEN-GEQGT----G---W--------AFAP---LTTEN 585 608  2833377 556 GLRDTV---------EN-FNPFAEK-GEQGT----G---W--------AF 579 609  1549232 556 GLRDTV---------EN-FNPFAEK-GEQGT----G---W--------AF 579 610  5295947 556 GLRDTV---------EN-FNPFAEK-GEQGT----G---W--------AF 579 611  6136121 507 GLVDTV---------TEGFTGF----HMGAF----NVECA--------TVDP---ADVQK 538 612  5441242 505 GLVDTV---------QEGFTGF----HMGAF----NVDCE--------AIDP---ADVEK 536 613  2833388 507 GLVDTV---------KEGYTGF----QMGAL----H---V--------ECDKIDSADVAA 538 614  3832512 506 GLVDTV---------KEGYTGF----HVGAF----SVECE--------AVDP---ADVEK 537 615 15223331 509 GLVDTV---------KDGYTGF----HIGRF----N---V--------KCEV---VDPDD 537 616  2833383 502 GLVDTVKEGYTGFHAGP-FDVE----CE--------------------DVDP---DDVDK 533 617 15637079 507 GLVDTV---------KEGYTGF----HMGAF----NVDCE--------TVDP---EDVLK 538 618   297196 506 GLVDTV---------KEGYTGF----HMGAF----N---VECD-----VVDP---ADVLK 537 619   228210 506 GLVDTV---------KEGYTGF----HMGAF----N---VECD-----VVDP---ADVLK 537 620   602594 506 GLVDTV---------KEGYTGF----HMGAF----N---VECD-----VVDP---ADVLK 537 621  2833381 507 GLVDTV---------KEGYTGF----HMGAF----NVDCE--------TVDP---EDVLK 538 622 12003285 503 GLVDTV---------KEGFTGF----HMGAF----N---VECD-----AVDP---ADVLK 534 623 15626365 512 GLVDTV---------KEGFTGF----HMGSF----N---V--------KCDA---VDPVD 540 624  6624281 503 GLVDTI---------VE---------GKTGF----H---MGRLSVDCNVVEP---ADVKK 534 625  6624287 503 GLVDTI---------VE---------GKTGF----H---MGRLSVDCNVVEP---ADVKK 534 626  4760584 503 GLVDTI---------VE---------GKTGF----H---MGRLSVDCNVVEP---ADVKK 534 627 18139611 507 GLVDTV---------KE-GVTG----FHMGLFNVEC---E--------TVDP---VDVTA 538 628 17736918 433 GLVDTI---------VE---------GKTGF----H---MGRLSVDCNVVEP---ADVKK 464

[0396] TABLE XXIII Maize soluble starch synthase IIa (SSIIa) “GLYTR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)              Sequence              end # 629 MaizeSSIIa 682 LIEALRHCLDTYRKYGES-WKSLQARGMSQDLSWDHAAELYEDVLVKAKYQW 732 630  7489710 682 LIEALRHCLDTYRKYGES-WKSLQARGMSQDLSWDHAAELYEDVLVKAKYQW 732 631  8953571 748 LIEALGHCLRTYRDYKES-WRGLQERGMSQDFSWEHAAKLYEDVLVKAKYQW 798 632  8953571 749 LIEALGHCLRTYRDYKES-WRGLQERGMSQDFSWEHAAKLYEDVLLKAKYQW 799 633  5825480 749 LIEALGHCLRTYRDYKES-WRGLQERGMSQDFSWEHAAKLYEDVLLKAKYQW 799 634  7529653 749 LIEALGHCLRTYRDFKES-WRALQERGMSQDFSWEHAAKLYEDVLVKAKYQW 799 635 16265834 760 LIEALGHCLETYRKYKES-WRGLQVRGMSQDLSWDHAAELYEEVLVKAKYQW 810 636  7489695 441 LIEALGHCLRTYRDFKES-WRALQERGMSQDFSWEHAAKLYEDVLVKAKYQW 491 637 15384987 587 MIDALGHCLNTYRNYKES-WRGLQARGMAQDLSWDHAAELYEDVLVKAKYQW 637 638 15028467 644 MIDALGHCLNTYRNYKES-WRGLQARGMAQDLSWDHAAELYEDVLVKAKYQW 694 639  7489711 648 MIDALSHCLTTYRNYKES-WRACRARGMAEDLSWDHAAVLYEDVLVKAKYQW 698 640  2833384 702 LMAALWNCLLTYKDYKKS-WEGIQERGMSQDLSWDNAAQQYEEVLVAAKYQW 752 641  2129898 702 LMAALWNCLLTYKDYKKS-WEGIQERGMSQDLSWDNAAQQYEEVLVAAKYQW 752 642  6467503 701 LIHALGNCLLTYREYKKS-WEGLQRRGMTPNLSWDHAAEKYEETLVAAKYQW 751 643 15232051 742 LIHALGNCLLTYREYKES-WEGLQRRGMTQDLSWDNAAEKYEEVLVAAKYHW 792 644  3192881 580 LIDALGNCLLTYRQYKQS-WEGLQRRGMMQDLSWDHAAEKYEEVLVAAKYQW 630 645  2833390 738 LIPRIRNCLLTYREYKKS-WEGIQTRCMTQDLSWDNAAQNYEEVLIAAKYQW 788 646 14495348 699 LIDALGHCLNTYRNYRTS-WEGLQKRGMMQDLSWDNAAKLYEEVLLAAKYQW 749 647  8708896 526 LRESINNALYTYRQFRDS-FRGIQRRGMEQDLTWDNAASIYEEVLVAAKYQW 576 648  2833387 447 MLWALRTAMSTFRENKPS-WEGLMKRGMTKDHTWDHA 482 649 15237934 598 MVSALRLAAATYREYKQS-WEGLMRRGMTRNYSWENAAVQYEQV-----FQW 643 650  5880466 593 MLWALRTAMSTFREHKPS-WEGLMKRGMTKDHTWDHAAEQYEQI 635 651  6690399 521 MVSALRLAAATYREYKQS-WEGLMRRGMTRNYSWENAAVQYEQV-----FQW 566 652  9369334 593 MLWALRTAMSTFREHKPS-WEGLMKRGMTKDHTWDHAAEQYEQI 635 653  6103327 593 MLWALRTAMSTFREHKPS-WEGLMKRGMTKDHTWDHAAEQYEQI 635 654  7188796 589 MLWALRTAISTFREHKPS-WEGLMKRGMTKDHTWDHAAEQYEQI 631 655  2829792 587 LLDTLKLAIGTYTEHKSS-WEGLMRRGMGRDYSWENAAIQYEQVFTWA 633 656  7484400 272 LRESINNALYTYRQFRDS-FRGIQRRGMEQDLTWDNAASIYEEVLVAAKYQW 322 657 12019656 593 MFVDIANC 600 658  7489712 586 MFVDIANC 593 659  6136121 539 IATTVERALAAYGSV--A-YKEMIQNCMAQDLSWKGPAKNWEKMLL 581 660  5441242 537 IATTVRRALGTYGTV--A-MEKIIQNCMAQDFSWKGPAKQWEKVL 578 661  2833388 539 IVKTVARALGTYAT--AA-LREMILNCMAQDLSWKGPARMWEKMLL 581 662  3832512 538 LATTVNRALKTYGT--QA-LKEMILNCMAQDFSWKGPAKQWEQALL 580 663 15223331 538 VIATAKAVTRAVAVYGTSAMQEMVKNCMDQDFSWKGPARLWEKVLL 583 664  2833383 534 LAATVKRALKTYGT--QA-MKQIILNCMAQNFSWKKPAKIWEKALL 576 665 15637079 539 VITTVGRALAMYGTL--A-FTEMIKNCMSQELSWKGPAKNWETVLL 581 666   297196 538 IVTTVARALAVYGTL--A-FAEMIKNCMSEELSWKEPAKKWETLLL 580 667   228210 538 IVTTVARALAVYGTL--A-FAEMIKNCMSEELSWKEPAKKWETLLL 580 668   602594 538 IVTTVARALAVYGTL--A-FAEMIKNCMSEELSWKEPAKKWETLLL 580 669  2833381 539 VITTVGRALAIYGTL--A-FTEMIKNCMSQELSWKGPAKNWETVLL 581 670 12003285 535 IVKTVGRALEVYGT--PA-FREMINNCMSLDLSWKGPAKNWETVLL 577 671 15626365 541 VDAIPKTVTKALGVYGTSAFAEMIKNCMAQELSWKGPAKYWEEVLL 586 672  6624281 535 VVTTLKRAVKVVGT--PA-YHEMVKNCMIQDLSWKGPAKNWEDVLLE 578 673  6624287 535 VVTTLKRAVKVVGT--PA-YHGMVKNCMIQDLSWKGPAKNWEDVLLE 578 674  4760584 535 VVTTLKRAVKVVGT--PA-YHEMVKNCMIQDLSWKGPAKNWEDVLLE 578 675 18139611 539 VASTVKRALKQYNT--PA-FQEMVQNCMAQDLSWKGPAKKWEEVLL 581 676 17736918 465 VVTTLKRAVKVVGT--PA-YHEMVKNCMIQDLSWKGPAKNWEDVLLE 508

[0397] TABLE XXIV Identities of the Accession Numbers used in Tables. XIX-XXIV. Accession Brief Description of sequences score Id. producing significant alignments (bits) E-value gi|7489710|pir| |T01208 ADPglucose--starch glucosyltransfera . . . 1389 0.0 gi|8953573|emb|CAB96627.1 (AJ269504) starch synthase IIa-3 . . . 976 0.0 gi|8953571|emb|CAB96626.1 (AJ269503) starch synthase IIa-2 . . . 976 0.0 gi|5825480|gb|AAD53263.1|AF155217_1 (AF155217) starch synth . . . 975 0.0 gi|7529653|emb|CAB86618.1| (AJ269502) starch synthase IIa-1 . . . 970 0.0 gi|16265834|gb|AAL16661.1|AF419099_1 (AF419099) putative so . . . 968 0.0 gi|7489695|pir| |T06798 probable starch synthase (EC 2.4.1.- . . . 910 0.0 gi|15384987|emb|CAC59826.1| (AJ308110) soluble starch synth . . . 902 0.0 gi|15028467|gb|AAK81729.1|AF395537_1 (AF395537) soluble sta . . . 892 0.0 gi|7489711|pir| |T01209 ADPglucose--starch glucosyltransfera . . . 863 0.0 gi|2833384|sp|Q43093|UGS3 PEA Glycogen [starch] synthase, c . . . 836 0.0 gi|2129898|pir| |S61505 UDPglucose--starch glucosyltransfera . . . 835 0.0 gi|6467503|gb|AAF13168.1|AF173900_1 (AF173900) granule boun . . . 832 0.0 gi|115232051|ref|(NP 186767.1| (NM_110984) putative glycogen . . . 826 0.0 gi|3192881|gb|AAC19119.1| (AF068834) starch synthase [Ipomo . . . 813 0.0 gi|2833390|sp|Q43847|UGS3 SOLTU Glycogen [starch] synthase, . . . 788 0.0 gi|14495348|gb|AAK64284.1|AF383878_1 (AF383878) soluble sta . . . 786 0.0 gi|8708896|gb|AAC17970.21 (AF026421) soluble starch synthas . . . 692 0.0 gi|2833387|sp|Q43654|UGS2 WHEAT Soluble glycogen [starch] s . . . 448  e−125 gi|15237934|ref|NP 197818.1| (NM_122336) soluble starch syn . . . 446  e−124 gi|5880466|gb|AAd54661.1| (AF091803) starch synthase I [Tri . . . 444  e−123 gi|6690399|gb|AAF24126.1|AF121673_1 (AF121673) soluble star . . . 444  e−123 gi|9369334|emb|CAB99209.1| (AJ292521) starch synthase I-1 [ . . . 444  e−123 gi|6103327|gb|AAF03557.1| (AF091802) starch synthase I [Aeg . . . 442  e−123 gi|7188796|gb|AAF37876.1|AF234163_1 (AF234163) starch synth . . . 441  e−122 gi|2829792|sp|P93568|UGS2 SOLTU Soluble glycogen [starch] s . . . 440  e−122 gi|7484400|pir| |T07924 probable starch synthase (EC 2.4.1.- . . . 428  e−119 gi|12019656|gb|AAd45815.2| (AF168786) soluble starch syntha . . . 412  e−114 gi|7489712|pir| |T01414 AdPglucose--starch glucosyltransfera . . . 407  e−112 gi|2833377|sp|Q40739|UGS2 ORYSA Soluble glycogen [starch] s . . . 391  e−107 gi|1549232|dbj|BAA07396.1| (D38221) SSS1 [Oryza sativa] >gi . . . 390  e−107 gi|5295947|dbj|BAA81848.1| (AB026295) ESTs AU075322 (C11109) . . . 390  e−107 gi|6136121|sp|082627|UGST ANTMA Granule-bound glycogen [sta . . . 350 3e−95 gi|5441242|dbj|BAA82346.1| (AB029546) granule-bound starch . . . 344 2e−93 gi|2833388|sp|Q43784|UGST MANES Granule-bound glycogen [sta . . . 342 9e−93 gi|3832512|gb|AAC70779.1| (AF097922) granule-bound glycogen . . . 338 9e−92 gi|15223331|ref|Np_174566.1| (NM_103023) starch synthase, p . . . 337 4e−91 gi|2833383|sp|Q43092|UGST PEA Granule-bound glycogen [starc . . . 334 2e−90 gi|15637079|dbj|BA968126.1| (AB071604) granule-bound starch . . . 333 5e−90 gi|2671961|sp|Q00775|UST SOLTU Granule-bound glycogen [star . . . 332 1e−89 gi|228210|prf| |11718316A granule-bound starch synthase [Sola . . . 330 2e−89 gi|602594|emb|CAA58220.1| (X83220) starch (bacterial glycog . . . 330 2e−89 gi|2833381|sp|Q42857|UGST IPOBA Granule-bound glycogen [sta . . . 327 2e−88 gi|12003285|9b|AAG43519.1|AP210699_1 (AF210699) granule-bou . . . 327 2e−88 gi|15626365|emb|CAC69955.1| (AJ345045) granule-bound starch . . . 327 3e−88 gi|6624281|dbj|BAA88509.1| (AB029061) starch synthase (GBSS . . . 320 4e−86 gi|6624287|dbj|BAA88512.1| (A3029064) starch synthase (GBSS . . . 319 7e−86 gi|4760584|dbj|BAA77352.1| (AB019624) starch synthase (GBSS . . . 318 1e−85 gi|18139611|gb|AAL58572.1| (AY069940) granule binding starc . . . 318 1e−85 gi|17736918|gb|AA41028.1| (AF2S0137) mutant granule bound . . . 318 1e−85 gi|6318538|gb|AAF06936.1|AF110373_1 (AF110373) granule-boun . . . 318 2e−85 gi|6624285|dbj|BAA88511.1| (AB029063) starch synthase (GBSS . . . 317 4e−85 gi|6318540|gb|AAF06937.1|AF110374_1 (AF110374) granule-boun . . . 316 5e−85 gi|4760582|dbj|BAA77351.1| (AB019623) starch synthase (GBSS . . . 316 5e−85 gi|11037536|gb|AAG27624.1|AF286320_1 (AF286320) granule bou . . . 316 6e−85 gi|136765|sp|P27736|UGST WHEAT Granule-bound glycogen [star . . . 314 2e−84 gi|4760580|dbj|BAA77350.1| (AB019622) starch synthase (GESS . . . 313 4e−84 gi|136755|sp|P09842|UGST HORVU Granule-bound glycogen [star . . . 313 4e−84 gi|18652407|gb|AAL77109.1|AF474373_6 (AF474373) granule-bon . . . 313 5e−84 gi|2833385|sp|Q43134|UGST SORBI Granule-bound glycogen [sta . . . 313 5e−84 gi|6492245|gb|AAF14233.1|AF109395_1 (AF109395) granule-boun . . . 312 8e−84 gi|6624283|dbj|BAA88510.11 (AB029062) starch synthase (GBSS . . . 311 1e−83 gi|4588609|gb|AAD26156.1|AF113844_1 (AF113844) granule-boun . . . 311 2e−83 gi|16716335|gb|AAC17969.3| (AF026420) granule-bound starch . . . 309 7e−83 gi|82478|pir| |JQ0703 UDPglucose--starch glucosyltransferasa . . . 308 9e−83 gi|2833382|sp|Q42968|UGST ORYGL Granule-bound glycogen [sta . . . 307 2e−82 gi|297424|emb|CAA46294.1|(X65183) glycogen (starch) syntha . . . 306 5e−82 gi|136757|sp|P047l3 UGST MAIZE Granule-bound glycogen [star . . . 306 5e−82 gi|7798551|gb|AAC61675.2| (AF031162) granule-bound starch s . . . 306 7e−82 gi|136758|sp|P19395|UGST ORYSA Granule-bound glycogen [star . . . 305 8e−82 gi|297422|emb|CAA45472.1| (X64108) starch granule-hound sta . . . 301 2e−80 gi|4588607|gb|AAD26155.1|AF113843_1 (AF113843) granule-boun . . . 293 4e−78 gi|15643657|ref|NP_228703.1| (NC_000853) glycogen synthase . . . 284 2e−75 gi|15900991|ref|NP_345595.1| (NC_003028) glycogen synthase . . . 283 4e−75 gi|15903076|ref|NP_358626.1| (NC_003098) Glycogen synthase . . . 283 5e−75 gi|15672681|ref|NP_266855.1| (NC_002662) glycogen synthase . . . 273 4e−72 gi|17366711|sp|Q9CEM9|GLGA LACLA Glycogen synthase (Starch . . . 272 8e−72 gi|18309046|ref|NP_560980.1| (NC_003366) glycogen synthase . . . 264 2e−69 gi|16080147|ref|NP_390973.1| (NC_000964) starch (bacterial . . . 263 6e−69 gi|15895507|ref|NP_348856.1| (NC_003030) Glycogen synthase, . . . 261 2e−68 gi|2811062|sp|008328|GLGA BACST Glycogen synthase (Starch [ . . . 257 2e−67 gi|17229371|ref|NP_485919.1| (NC_003272) glycogen synthase . . . 251 2e−65 gi|15613648|ref|NP_241951.1| (NC_002570) starch (bacterial . . . 248 1e−64 gi|1641730|ref|NP_231362.1| (NC_002505) glycogen synthase . . . 234 2e−60 gi|16766821|ref|NP_462436.1| (NC_003197) glycogen synthase . . . 233 5e−60 gi|16331219|ref|NP_441947.1| (NC_000911) glycogen synthase . . . 231 2e−59 gi|15620537|gb|AAL03921.1|U30252_9 (U30252) GlgA [Synechoco . . . 231 3e−59 gi|16762766|ref|NP_458383.1| (NC_003198) glycogen synthase . . . 231 3e−59 gi|17938870|ref|NP_535658.1| (NC_003306) glycogen synthase . . . 222 1e−56 gi|16119514|ref|NP_396220.1| (NC_003064) AGR_pAT_410p [Agro . . . 221 1e−56 gi|16124067|ref|NP_407380.1| (NC_003143) glycogen synthase . . . 219 6e−56 gi|6116748|dbj|BAA85761.1| (AB028026) granule-bound starch . . . 219 7e−56 gi|15803938||ref NP_289974.1| (NC_002655) glycogen synthase . . . 219 1e−55 gi|15966599|ref|NP_386952.1| (NC_003047) PROBABLE GLYCOGEN . . . 217 4e−55 gi|15890897|ref|NP_356569.1| (NC_003063) AGR_L_1562p [Agrob . . . 216 8e−55 gi|13476305|ref|NP_107875.1| (NC_002678) glycogen synthase . . . 215 2e−54 gi|14279432|gb|AAK58595.1|AF268959_2 (AF268969) glycogen sy . . . 214 4e−54 gi|17366749|sp|Q9EUT5|GLGA_RHITR Glycogen synthase (Starch . . . 213 5e−54 gi|15717885|gb|AAK97773.1| (AY044844) starch synthase isofo . . . 213 7e−54 gi|4582783|emb|CAB40375.1| (AJ006752) starch synthase, isof . . . 213 7e−54 gi|16329217|ref|NP_439945.1| (NC_000911) glycogen (starch) . . . 211 2e−53 gi|17227527|ref|NP_484075.1| (NC_003272) glycogen (starch) . . . 211 3e−53 gi|9587293|gb|AAF89248.1|AF285973_1 (A9285973) granule-boun . . . 209 8e−53 gi|9587321|gb|AAF89262.1|AF285987_1 (AF285987) granule-boun . . . 209 1e−52 gi|8901183|gb|AAC17971.2| (AF026422) soluble starch synthas . . . 208 1e−52 gi|15602409|ref|NP_245481.1| (NC_002663) GlgA [Pasteurella . . . 208 2e−52 gi|9587317|gb|AAF89260.1|AF285985_1 (AF285985) granule-boun . . . 207 5e−52 gi|9587301|gb|AAF89252.1|AF285977_1 (AF285977) granule-boun . . . 206 8e−52 gi|15605118|ref|NP_213495.1| (NC_000918) glycogen synthase . . . 205 2e−51 gi|146139|gb|AAA23870.1| (J02616) glycogen synthase (EC 2.4 . . . 204 2e−51 gi|16265159|ref|NP_437951.1| (NC_003078) putative glycogen . . . 204 2e−51 gi|9587329|gb|AAF89266.1|AF28599_1 (AF285991) granula-boun . . . 204 3e−51 gi|9587352|gb|AAF89276.1|AF286003_1 (AF286003) granula-boun . . . 203 7e−51 gi|9587311|gb|AAF89257.1|AF285982_1 (AF285982) granule-boun . . . 199 1e−49 gi|9587305|gb|AAF89254.1|AF285979 1 (AF285979) granule-boun . . . 198 1e−49 gi|9587343|gb|AAF89273.1|A9285998 1 (AF285998) granule-boun . . . 198 2e−49 gi|17548463|ref|NP_521803.1| (NC_003296) PROBABLE GLYCOGEN . . . 198 2e−49 gi|18461221|dbj|BAb84418.1| (AP003292) putative starch synt . . . 197 2e−49 gi|9587337|gb|AAF89270.1|AF285995_1 (AF285995) granule-boun . . . 197 3e−49 gi|16273270|ref|NP_439511.1| (NC_000907) glycogen synthase . . . 196 5e−49 gi|9587348|gb|AAF89274.1| (AF286001) granule-bound starch s . . . 196 5e−49 gi|9587341|gb|AAF89272.1|AF285997 1(AF285997) granule-boun . . . 196 6e−49 gi|9587323|gb|AAF89263.1|AF285988 1(AF285988) granule-boun . . . 196 7e−49 gi|15236819|ref|NP_193558.1| (NM 117934) starch synthase-li . . . 194 2e−48 gi|9587307|gb|AA989255.1|AF285980_1 (AF285980) granule-boun . . . 194 2e−48 gi|9587327|gb|AAF89265.1|AF285990_1 (AF285990) granule-boun . . . 194 3e−48 gi|9587319|gb|AAF89261.1|AF285986_1 (AF285986) granule-boun . . . 194 4e−48 gi|15983795|gb|AAL10494.1| (AY056803) Atlg32900/F9L11_8 [Ar . . . 193 5e−48 gi|9587313|gb|AAF89258.1|AF285983_1 (AF285983) granule-boun . . . 193 7e−48 gi|9587297|gb|AAF89250.1|AF285975_1 (AR285975) granule-boun . . . 193 7e−48 gi|9587309|gb|AAF89256.1|AF285981_1 (AF285981) granule-boun . . . 192 8e−48 gi|9587299|gb|AAF89251.1|AF285976_1 (AF285976) granule-boun . . . 192 8e−48 gi|9587333|gb|AAF89268.1|AF285993_1 (AF285993) granule-boun . . . 192 9e−48 gi|9587325|gb|AAF89264.1|AF285989_1 (AF285989) granule-boun . . . 191 2e−47 gi|5834407|gb|AAD53959.1|AF181035_3 (AF181035) glycogen syn . . . 191 3e−47 gi|17367070|sp|Q9RNH6|GLGA RHOSH Glycogen synthase (Starch . . . 191 3e−47 gi|15221083|ref|NP_172637.1| (NM_101044) putative glycogen . . . 190 4e−47 gi|15597361|ref|NP_250855.1| (NC_002516) probable glycogen . . . 189 1e−46 gi|9587331|gb|AAF89267.1|AF285992_1 (AF285992) granule-boun . . . 189 1e−46 gi|7489826|pir| |T01265 starch synthase DULL1 - maize >gi|30 . . . 188 2e−46 gi|9587303|gb|AAF89253.1|AF285978_1 (AF285978) granule-boun . . . 188 2e−46 gi|4582789|emb|CAB40374.1| (AJ225088) Starch synthase isofo . . . 188 2e−46 gi|9587339|gb|AAF89271.1|AF285996_1 (AP285996) granula-boun . . . 187 4e−46 gi|9587335|gb|AAF89269.1|AF285994_1 (AF285994) granule-boun . . . 187 4e−46 gi|9587295|gb|AAF89249.1|AF285974_1 (AF285974) granule-boun . . . 186 6e−46 gi|15805621|ref|NP_294317.1| (NC_001263) glycogen synthase . . . 184 4e−45 gi|17367076|sp|Q9RWS1|GLGA DEIRA Glycogen synthase (Starch . . . 183 6e−45 gi|7489274|pir| |T07663 soluble starch synthase (EC 2.4.1.-) . . . 183 7e−45 gi|2833389|sp|Q43846|UGS4 SOLTU Soluble glycogen [starch]s . . . 181 3e−44 gi|9502145|gb|AAF88000.1| (AF258609) starch synthase III [A . . . 179 8e−44 gi|9502143|gb|AAF87999.1|AF258608_1 (AF258608) starch synth . . . 177 2e−43 gi|7484399|pir| |T07926 probable starch synthase (EC 2.4.1.- . . . 177 3e−43 gi|17366350|sp|P58395|GLGA THECA Glycogen synthase (Starch . . . 176 5e−43 gi|17646328|gb|AAL40942.1 AF432915_1 (AF432915) putative st . . . 175 1e−42 gi|12278503|gb|AAG48992.1| (AY011005) granule-bound starch . . . 170 5e−41 gi|3493007|gb|AAD02961.1| (AF079241) granule-bound starch s . . . 170 6e−41 gi|12278507|gb|AAG48994.1| (AY011007) granule-bound starch . . . 170 6e−41 gi|3493065|gb|AAD02990.1| (AF079270) granule-bound starch s . . . 169 8e−41 gi|3493055|gb|AAD02985.1| (AF079265) granule-bound starch s . . . 169 1e−40 gi|3493079|gb|AAD02997.1| (AF079277) granule-bound starch s . . . 169 1e−40 gi|12278417|gb|AAG48949.1| (AY010962) granule-bound starch . . . 169 1e−40 gi|3493057|gb|AAD02986.1| (AF079266) granule-bound starch s . . . 169 1e−40 gi|3493061|gb|AAD02988.1| (AF079268) granule-bound starch s . . . 169 1e−40 gi|12278505|gb|AAG48993.1| (AY011006) granule-bound starch . . . 169 1e−40 gi|3493059|gb|AAD02987.1| (AF079267) granule-bound starch s . . . 169 1e−40 gi|3493107|gb|AAD03011.1| (AF079291) granule-bound starch s . . . 168 2e−40 gi|3493049|gb|AAD02982.1| (AF079262) granule-bound starch s . . . 168 2e−40 gi|12278487|gb|AAG48984.1| (AY010997) granule-bound starch . . . 168 2e−40 gi|3493089|gb|AAD03002.1| (AF079282) granule-bound starch . . . 168 2e−40 gi|12278473|gb|AAG48977.1| (AY010990) granule-bound starch . . . 168 2e−40 gi|3493051|gb|AAD02983.1| (AF079263) granule-bound starch s . . . 167 2e−40 gi|12278427|gb|AAG48954.1| (AY010967) granule-bound starch . . . 167 3e−40 gi|12278497|gb|AAG48989.1| (AY011002) granule-bound starch . . . 167 3e−40 gi|3493005|gb|AAD02960.1| (AF079240) granule-bound starch s . . . 167 3e−40 gi|12278463|gb|AAG48972.1| (AY010985) granule-bound starch . . . 167 3e−40 gi|12278509|gb|AAG48995.1| (AYO11008) granule-bound starch . . . 167 3e−40 gi|3493093|gb|AAD03004.1| (AF079284) granule-bound starch s . . . 167 3e−40 gi|3493073|gb|AAD02994.1| (AF079274) granule-bound starch s . . . 167 4e−40 gi|12278471|gb|AAG48976.1| (AY010989) granule-bound starch . . . 167 4e−40 gi|3493019|gb|AAD02967.1| (AF079247) granule-bound starch s . . . 167 5e−40 gi|12278453|gb|AAG48967.1| (AY010980) granule-bound starch . . . 167 5e−40 gi|12278491|gb|AAG48986.1| (AY010999) granule-bound starch . . . 166 6e−40 gi|12278451|gb|AAG48966.1| (AY010979) granule-bound starch . . . 166 6e−40 gi|3493077|gb|AAD02996.1| (AF079276) granule-bound starch s . . . 166 7e−40 gi|3493067|gb|AAD02991.1| (AF079271) granule-bound starch s . . . 166 7e−40 gi|3493097|gb|AAD03006.1| (AF079286) granule-bound starch s . . . 166 7e−40 gi|12278514|gb|AAG48997.1| (AY011011) granule-bound starch . . . 166 7e−40 gi|3493121|gb|AAD03018.1| (AF079298) granule-bound starch s . . . 166 8e−40 gi|3493091|gb|AAD03003.1| (AF079283) granule-bound starch s . . . 166 8e−40 gi|12278481|gb|AAG48981.1| (AY010994) granule-bound starch . . . 166 8e−40 gi|3493083|gb|AAD02999.1| (AF079279) granule-bound starch s . . . 166 8e−40 gi|3493111|gb|AAD03013.1| (AF079293) granule-bound starch s . . . 166 8e−40 gi|12278457|gb|AAG48969.1| (AY010982) granule-bound starch . . . 166 9e−40 gi|13774482|gb|AAK38880.1| (AF353518) granule-bound starch . . . 166 9e−40 gi|12278479|gb|AAG48980.1| (AY010993) granule-bound starch . . . 166 9e−40 gi|3493095|gb|AAD03005.1| (AF079285) granule-bound starch s . . . 166 1e−39 gi|3493081|gb|AAD02998.1| (AF079278) granule-bound starch s . . . 166 1e−39 gi|112278429|gb|AA048955.1| (AY010968) granule-bound starch . . . 166 1e−39 gi|3493087|gb|AAD03001.1| (AF079281) granule-bound starch s . . . 166 1e−39 gi|12278485|gb|AAG48983.1| (AY010996) granule-bound starch . . . 166 1e−39 gi|3493025|gb|AAD02970.1| (AF079250) granule-bound starch s . . . 165 1e−39 gi|13774486|gb|AAK38882.1| (AF353520) granule-bound starch . . . 165 1e−39 gi|3493117|gb|AAD03016.1| (AF079296) granule-bound starch s . . . 165 1e−39 gi|12278425|gb|AAG48953.1| (AY010966) granule-bound starch . . . 165 2e−39 gi|3493031|gb|AAD02973.1| (AF079253) granule-bound starch s . . . 164 2e−39 gi|12278499|gb|AAG48990.1| (AY011003) granule-bound starch . . . 164 3e−39 gi|12278443|gb|AAG48962.1| (AY010975) granule-bound starch . . . 164 3e−39 gi|12278511|gb|AAG48996.1| (AY011009) granule-bound starch . . . 164 3e−39 gi|12278495|gb|AAG48988.1| (AY011001) granule-bound starch . . . 164 3e−39 gi|3493099|gb|AAD03007.1| (AF079287) granule-bound starch s . . . 164 3e−39 gi|12278411|gb|AAG48946.1| (AY010959) granule-bound starch . . . 164 3e−39 gi|13377473|gb|AAK20725.1| (AF318769) granule-bound starch . . . 164 3e−39 gi|12278501|gb|AAG48991.1| (AY011004) granule-bound starch . . . 164 3e−39 gi|12278449|gb|AAG48965.1| (AY010978) granule-bound starch . . . 164 4e−39 gi|3493103|gb|AAD03009.1| (AF079289) granule-bound starch s . . . 164 4e−39 gi|12278477|gb|AAG48979.1| (AY010992) granule-bound starch . . . 164 4e−39 gi|12278423|gb|AAG48952.1| (AY010965) granule-bound starch . . . 164 4e−39 gi|122784211|gb|AAG48951.1| (AY010964) granule-bound starch . . . 164 4e−39 gi|12278489|gb|AAG48985.1| (AY010998) granule-bound starch . . . 164 4e−39 gi|13774484|gb|AAK38881.1| (AF353519) granule-bound starch . . . 164 4e−39 gi|3493023|gb|AAD02969.1| (AF079249) granule-bound starch s . . . 164 4e−39 gi|13377475|gb|AAK20726.1| (AF318770) granule-bound starch . . . 164 4e−39 gi|12278435|gb|AAG48985.1| (AY010971) granule-bound starch . . . 164 4e−39 gi|12278469|gb|AAG48975.1| (AY010988) granule-bound starch . . . 163 5e−39 gi|3493101|gb|AAD03008.1| (AF079288) granule-bound starch s . . . 163 5e−39 gi|3493113|gb|AAD03014.1| (AF079294) granule-bound starch s . . . 163 5e−39 gi|12278419|gb|AAg48950.1| (AY010963) granule-bound starch . . . 163 6e−39 gi|3493071|gb|AAD02993.1| (AF079273) granule-bound starch s . . . 163 6e−39 gi|3493053|gb|AAD02984.1| (AF079264) granule-bound starch s . . . 163 6e−39 gi|3493075|gb|AAD02995.1| (AF079275) granule-bound starch s . . . 163 7e−39 gi|12278475|gb|AAG48978.1| (AY010991) granule-bound starch . . . 162 8e−39 gi|3493041|gb|AAG42978.1| (AF079258) granule-bound starch s . . . 162 9e−39 gi|12278433|gb|AAG48957.1| (AY010970) granule-bound starch . . . 162 9e−39 gi|3493037|gb|AAD02976.1| (AF079256) granule-bound starch s . . . 162 1e−38 gi|3493017|gb|AAD02966.1| (AF079246) granule-bound starch s . . . 162 1e−38 gi|3493015|gb|AAD02965.1| (AF079245) granule-bound starch s . . . 162 1e−38 gi|12278437|gb|AAG48959.1| (AY010972) granule-bound starch . . . 162 1e−38 gi|3493021|gb|AAD02968.1| (AF079248) granule-bound starch s . . . 162 1e−38 gi|3493069|gb|AAD02992.1| (AF079272) granule-hound starch s . . . 162 1e−38 gi|3493027|gb|AAD02971.1| (AF079251) granule-bound starch s . . . 161 2e−38 gi|3493013|gb|AAD02964.1| (AF079244) granule-bound starch s . . . 161 2e−38 gi|3493011|gb|AAD02963.1| (AF079243) granule-bound starch s . . . 161 2e−38 gi|12278493|gb|AAG48987.1| (AY011000) granule-bound starch . . . 161 2e−38 gi|12278413|gb|AAG48947.1| (AY010960) granule-bound starch . . . 161 2e−38 gi|3493085|gb|AAD03000.1| (AF079280) granule-bound starch s . . . 161 3e−38 gi|3493009|gb|AAD02962.1| (AF079242) granule-bound starch s . . . 161 3e−38 gi|3493035|gb|AAD02975.1| (AF079255) granule-bound starch s . . . 160 4e−38 gi|3493063|gb|AAD02989.1| (AF079269) granule-bound starch s . . . 160 4e−38 gi|12278431|gb|AAG48956.1| (AY010969) granule-bound starch . . . 160 4e−38 gi|3492999|gb|AAD02957.1| (AF079237) granule-bound starch s . . . 160 5e−38

[0398] SSIIb Accession: AF019297       NID: g2655030            Mol. wt. (calc) = 75458      Residues = 698 SEQ.ID. No. 677 1 M P G A I S S S S S A F L L P V A S S S P R R R R G S V G A 31 A L R S Y G Y S G A E L R L H W A R R G P P Q D G A A S V R 61 A A A A P A G G E S E E A A K S S S S S Q A G A V Q G S T A 91 K A V D S A S P P N P L T S A P K Q S Q S A A M Q N G T S G 121 G S S A S T A A P V S G P K A D H P S A P V T K R E I D A S 151 A V K P E P A G D D A R P V E S I G I A E P V D A K A D A A 181 P A T D A A A S A P Y D R E D N E P G P L A G P N V M N V V 211 V V A S E C A P F C K T G G L C D V V G A L P K A L A R R G 241 H R V M V V I P R Y G E Y A E A R D L G V R R R Y K V A G Q 271 D S E V T Y F H S Y I D G V D F V F V E A P P F R H R H N N 301 I Y C G E R L D I L K R M I L F C K A A V E V P W Y A P C G 331 G T V Y G D G N L V F I A N D W H T A L L P V Y L K A Y Y R 361 D N G L M Q Y A R S V L V I H N I A H Q G R G P V D D F V N 391 F D L P E H Y I D H F K L Y D N I G G D H S N V F A A G L K 421 T A D R V V T V S N G Y M W E L K T S E G G W G L H D I I N 451 Q N D W K L Q G I V N G I D M S E W N P A V D V H L H S D D 481 Y T N Y T F E T L D T G K R Q C K A A L Q R Q L G L Q V R D 511 D V P L I G F I G R L D H Q K G V D I I A D A I H W I A G Q 541 D V Q L V M L G T G R A D L E D M L R R F E S E H S D K V R 571 A W V C F S V P L A H R I T A G A D I L L M P S R F E P C G 601 L N Q L Y A M A Y G T V P V V H A V G G L R D T V A P F D P 631 F N D T G L G W T F D R A E A N R M I D A L S H C L T T Y R 661 N Y K E S W R A C R A R G M A E D L S W D H A A V L Y E D V 691 L V K A K Y Q W

[0399] TABLE XXV Maize soluble starch synthase IIb (SSIIb) Alignments with other similar proteins-Transit Peptide SEQ Accession a.a a.a. Id.No. Number # (start)                  Sequence                  ending # 678 MAIZE SSIIb 1 MPGAISSSSSAFL-LXXXXXXXXXXXXXXXXALRSYGYSGAELRLHWARRGPPQDXXXXX 59 679  7489711 1 MPGAISSSSSAFL-LPVASSSPRRRRGSVGAALRSYGYSGAELRLHWARRGPPQDGAASV 59 680 15028467 1 MSGAIASSPAATLFLAGSSSSSPRRRRSRVSGVWWHLYGGTGLRLHWERRGLVRDGAVVC 60 Cont . . . d 678 Maize SSIIb 61 XXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXKAVDSASPPNPLTSAPKQSQSA-AMQNXX 118 679  7489711 60 RAAAAPAGGESEEAAKSSSSSQAGAVQGSTAKAVDSASPPNPLTSAPKQSQSA-AMQNGT 118 680 15028467 61  SASAAGGEDGVAKAKTKSAGSSKAVAVQGSTAKADHVEDS---VSSPKYVKPAVAKQNGE 117 681 15384987 45                                              SSPKSVKPAVAKQNGE 60 Cont . . . d 678 Maize SSIIb 119 XXXXXXXXXXPVSGPKADHPSAPVTKREID--ASAVKPEPAGDDARPVESIGIXXXXXXX 176 679  7489711 119  SGGSSASTAAPVSGPKADHPSAPVTKREID--ASAVKPEPAGDDARPVESIGIAEPVDAK 176 680 15028467 118  VVSRATKSDAPVSKPKVD-PSVPASKAEADGNAQAVESKAALDKK---EDVGVAEPLEAK 173 681 15384987 61  VVSRATKSDAPVPKPKVD-PSVPASKAEADGNAQAVESKAALDKK---EDVGVAEPLEAK 116

[0400] TABLE XXVI Maize soluble starch synthase IIb (SSIIb) “GLASS” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start                   Sequence                   end # 682 MaizeSSIIb 177 XXXXXXXXXXXXXXYDREDNEPGPLAGPNV-----MNVVVVASECAPFCKTGGLGDVVGA 231 683  7489711 177 ADAAPATDAAASAPYDREDNEPGPLAGPNV-----MNVVVVASECAPFCKTGGLGDVVGA 231 684 15028467 174 ADAGGDAGAVSSAD-DSENKESGPLAGPNV-----MNVIVVASECSPFCKTGGLGDVVGA 227 685 15384987 117 ADAGGDAGAVSSAD-DSENKESGPLAGPNV-----MNVIVVASECSPFCKTGGLGDVVGA 170 686  7489710 229                   DNDSGPLAGENV-----MNVIVVAAECSPWCKTGGLGDVVGA 265 687 16265834 306                  QDDDSGPLAGENV-----MNVIVVAAECSPWCKTGGLGDVAGA 343 688 15232051 287                 KDEEKPPPLAGANV-----MNVILVAAECAPFSKTGGLGDVAGA 325 689  7489695 1                                     NVVVVAAECSPWCKTGGLGDVAGA 24 690  6467503 247                  EDMKPPPLAGDNV-----MNVILVAAECAPWSKTGGLGDVAGS 284 691  2833384 245               FESGGEKPPPLAGTNV-----MNIILVSAECAPWSKTGGLGDVAGS 285 692  2129898 245               FESGGEKPPPLAGTNV-----MNIILVSAECAPWSKTGGLGDVAGS 285 693  3192881 126                  EDLKPPPLAGTNV-----MNVILVCAECAPWSKTGGLGDVAGA 163 694  8953571 294                  QNHDSGPLAGENV-----MNVVVVAAECSPWCKTGGLGDVAGA 331 695  7529653 295                  QNHDSGPLAGENV-----MNVVVVAAECSPWCKTGGLGDVAGA 332 696  8953571 295                  QNHDSGPLAGENV-----MNVVVVAAECSPWCKTGGLGDVAGA 332 697  5825480 295                  QNHDSGPLAGENV-----MNVVVVAAECSPWCKTGGLGDVAGA 332 698 14495348 247                    DDPSASASVDL-----INIILVAAECAPWSKTGGLGDVAGA 282 699  2833390 284                   DEKPPPLAGTNV-----MNIILVASECAPWSKTGGLGDVAGA 320 700  8708896 75                     KPPPLAGPNV-----MNVVMVGAECAPWSKTGGLGDVMAA 109 701  5880466 140                                     SIVFVTGEAAPYAKSGGLGDVCGS 163 702  9369334 140                                     SIVFVTGEAAPYAKSGGLGDVCGS 163 703 15237934 141                              V-----NNLVFVTSEAAPYSKTGGLGDVCGS 166 704  7188796 136                                     SIVFVTGEAAPYAKSGGLGDVCGS 159 705  6103327 140                                     SIVFVTGEAAPYAKSGGLGDVCGS 163 706  9369336 140                                     SIVFVTGEAAPYAKSGGLGDVCGS 163 707  6690399 64                              V-----NNLVFVTSEAAPYSKTGGLGDVCGS 89 708  2829792 118                DTEEMEETPIK--LT-----FNIIFVTAEAAPYSKTGGLGDVCGS 155 709  2833387 1                                            EAAPYAKSGGLGDVCGS 17 710 12019656 140                                     SIVFVTGEASPYAKSGGLGDVCGS 163 711  7489712 133                                     SIVFVTGEASPYAKSGGLGDVCGS 156 712  5295947 134                                     SVVFVTGEASPYAKSGGLGDVCGS 157 713  1549232 134                                     SVVFVTGEASPYAKSGGLGDVCGS 157 714  2833377 134                                     SVVFVTGEASPYAKSGGLGDVCGS 157 715  6136121 82                               -----MNLVFVLAEVGPWSKTGGLGDVVGG 106 716   228210 81                               -----MNLIFVGTEVGPWSKTGGLGDVLGG 105 717   297196 81                               -----MNLIFVGTEVGPWSKTGGLGDVLGG 105 718  2833388 82                               -----MNLIFVGAEVGPWSKTGGLGDVLGG 106 719 15637079 65                   ENEGGMAAGTIVCKQQGMNLVFVGCEVGPWCKTGGLGDVLGG 106 720   602594 81                               -----MNLIFVGTEVGPWSKTGGLGDVLGG 105 721  2833381 82                               -----MNLVFVGCEEGPWCKTGGLGDVLGG 106 722  5441242 80                               -----MNLIFVGAEVAPWSKTGGLGDVLGG 104 723 15223331 84                               -----MSVIFIGAEVGPWSKTGGLGDVLGG 108 724 12003285 78                               -----MTLIFVSAECGPWSKTGGLGDVVGG 102 725  3832512 79                             NG-----MNLVFVGAEVGPWSKTGGLGDVLGG 105 726 15626365 87                               -----MNLIFVGTEVAPWSKTGGLGDVLGG 111 727  2833383 77                               -----MSLVFVGAEVGPWSKTGGLGDVLGG 101 728  6624281 73                           GSGG-----MNLVFVGAEMAPWSKTGGLGDVLGG 101 729 17736918 3                           GSGG-----MNLVFVGAEMAPWSKTGGLGDVLGG 31 730  4760584 73                           GSGG-----MNLVFVGAEMAPWSKTGGLGDVLGG 101 731  6492245 63                      PAPIVCSTG-----MPIIFVATEVHPWCKTGGLGDVVGG 96 682 MaizeSSIIb 232 LPKALARRGHRVMVVIPRY-------GEYAEARDLG----VRRRYKVA--GQDSEVTYFH 278 683  7489711 232 LPKALARRGHRVMVVIPRY-------GEYAEARDLG----VRRRYKVA--GQDSEVTYFH 278 684 15028467 228 LPKALARRGHRVMVVIPRY-------GEYAEAKDLG----VRKRYRVA--GQDSEVSYFH 274 685 15384987 171 LPKALARRGHRVMVVIPRY-------GEYAEAKDLG----VRKRYRVA--GQDSEVSYFH 217 686  7489710 266 LPKALARRGHRVMVVVPRY-------GDYVEAFDMG----IRKYYKAA--GQDLEVNYFH 312 687 16265834 344 LPKALARRGHRVMVVVPRY-------GDYAEAQDVG----IRKYYKAA--GQDLEVKYFH 390 688 15232051 326 LPKSLARRGNRVMVVVPRY-------AEYAEAKDLG----VRKRYKVA--GQDMEVMYFH 372 689  7489695 25 LPKALAKRGHRVMVVVPRY-------GDYEEAYDVG----VRKYYKAA--GQDMEVNYFH 71 690  6467503 285 LPKALARRGHRVMVVAPRY-------GNYVEPQDTG----VRKRYKVD--GQDFEVSYFQ 331 691  2833384 286 LPKALARRGHRVMIVAPHY-------GNYAEAHDIG----VRKRYKVA--GQDMEVTYFH 332 692  2129898 286 LPKALARRGHRVMIVAPHY-------GNYAEAHDIG----VRKRYKVA--GQDMEVTYFH 332 693  3192881 164 LPKALARRGHRVMVVVPLY-------GNYAEPQHTG----VRKMFKID--GQDMEVNYFH 210 694  8953571 332 LPKALAKRGHRVMVVVPRY-------GDYEEAYDVG----VRKYYKAA--GQDMEVNYFH 378 695  7529653 333 LPKALAKRGHRVMVVVPRY-------GDYEEAYDVG----VRKYYKAA--GQDMEVNYFH 379 696  8953571 333 LPKALAKRGHRVMVVVPRY-------GDYEEAYDVG----VRKYYKAA--GQDMEVNYFH 379 697  5825480 333 LPKALAKRGHRVMVVVPRY-------GDYEEAYDVG----VRKYYKAA--GQDMEVNYFH 379 698 14495348 283 LPKALARRGURVMVVVPMY-------KNYAEPQQLG----EPRRYQVA--GQDMEVIYYH 329 699  2833390 321 LFKALARRGHRVMVVAPRY-------DNYPEPQDSG----VRKIYKVD--GQDVDVTYFQ 367 700  8708896 110 LPKALVRRGHRVMVVVPRY-------ENYDNAWETG----IRKIYSVF--NSNQEVGYFH 156 701  5880466 164 LPIALAARGHRVMVVMPRYLNGSSD-KNYAKALYTG----KHIKIPCF--GGSHEVTFFH 216 702  9369334 164 LPIALAARGHRVMVVMPRYLNGSSD-KNYAKALYTG----KHIKIPCF--GGSHEVTFFH 216 703 15237934 167 LPIALAGRGHRVMVISPRYLNGTAADKNYARAKDLG----IRVTVNCF--GGSQEVSFYH 220 704  7188796 160 LPIALAARGHRVMVVMPRYLNGTSD-KNYAKALYTG----KHIKIPCF--GGSHEVTFFH 212 705  6103327 164 LPIALAARGHRVMVVMPRYLNGSSD-KNYAKALYTA----KHIKIPCF--GGSHEVTFFH 216 706  9369336 164 LPIALAARGHRVMVVMPRYLNGSSD-KNYAKALYTA----YHIKIPCF--GGSHEVTFFH 216 707  6690399 90 LPIALAGRGHRVMVISPRYLNGTAADKNYAPAKDLG----IRVTVNCF--GGSQEVSFYH 143 708  2829792 156 LPMALAARGHRVMVVSPRYLNGGPSDEKYANAVDLD----VRATVHCF--GDAQEVAFYH 209 709  2833387 18 LPIALAARGHRVMVVMPRYLNGSSD-KNYAKALYTA----KHIKIPCF--GGSHEVTFFH 70 710 12019656 164 LPVALAARGHRVMVVMPRYLNGTSD-KNYANAFYTE----KHIRIPCF--GGEHEVTFFH 216 711  7489712 157 LPVALAARGHRVMVVMPRYLNGTSD-KNYANAFYTE----KHIRIPCF--GGEHEVTFFH 209 712  5295947 158 LPIALALRGHRVMVVMPRY-------MNGALNKNFANAFYTEKHIKIPCFGGEHEVTFFH 210 713  1549232 158 LPIALALRGHRVMVVMPRY-------MNGALNKNFANAFYTEKHIKIPCFGGEHEVTFFH 210 714  2833377 158 LPIALALRGHRVMVVMPRY-------MNGALNKNFANAFYTEKHIKIPCFGGEUEVTFFH 210 715  6136121 107 LPPAMAGNGHRVMTVSPRY-------DQYKDAWDTS----VVVEIKVG--DSIETVRFFH 153 716   228210 106 LPPALAARGHRVMTISPRY-------DQYKDAWDTS----VAVEVKVG--DSIEIVRFFH 152 717   297196 106 LPPALAARGHRVMTISPRY-------DQYKDAWDTS----VAVEVKVG--DSIEIVRFFH 152 718  2833388 107 LPPAMAARGHRVMTVSPRY-------DQYKDAWDTS----VSVEIKIG--DRIETVRFFH 153 719 15637079 107 LPPALAARGHRVMTVCPRY-------DQYKDAWDTC----VVVELQVG--DRIEPVRFFH 153 720   602594 106 LPPALAARGHRVMTISPRY-------DQYKDTWDTS----VAVEVKVG--DSIEIVRFFH 152 721  2833381 107 LPPALAARGHRVMTVCPRY-------DQYKDAWETC----VVVEPQVG--DRIEPVRFFH 153 722  5441242 105 LPSALAEHGHRVMTVSPRY-------DQYKDAWDTN----VTVEVKVA--DRIETVRFFH 151 723 15223331 109 LPPALAARGHRVMTICPRY-------DQYKDAWDTC----VVVQIKVG--DKVENVRFFH 155 724 12003285 103 LPPALAANRHRVMTVSPRY-------DQYKDAWDTS----VVVEIQVG--DKVETVGFFH 149 725  3832512 106 LPPALAGNGHRVMTVSPRY-------DQYKDAWDTG----VSVEIKVG--DRFETVRFFH 152 726 15626365 112 LPPALSANGHRVMTVTPRY-------DQYKDAWDTN----VTIEVKVG--DRTEKVRFFH 158 727  2833383 102 LPPVLAGNGHRVMTVSPRY-------DQYKDAWDTN----VLVEVKVG--DKIETVRFFH 148 728  6624281 102 LPAAMAANGHRVMVISPRY-------DQYKDAWDTS----VISEIKVV--DRYERVRYFH 148 729 17736918 32 LPPAMAANGHRVMVISPRY-------DQYKDAWDTS----VVSEIKVV--DKYERVRYFH 78 730  4760584 102 LPPAMAANGHRVMVISPRY-------DQYKDAWDTS----VVSEIKVV--DKYERVRYFH 148 731  6492245 97 LPPALAAMGHRVMTIAPRY-------DQYKDTWDTN----VLVEVIVG--DRTETVRFFH 143 682 MaizeSSIIb 279 SYIDGVDFVFVEAPPFRH---R---------HNNIY----G---G----ERLDILKRMIL 315 683  7489711 279 SYIDGVDFVFVEAPPFRH---R---------HNNIY----G---G----ERLDILKRMIL 315 684 15028467 275 AFIDGVDFVFLEAPPFRH---R---------HNDIY----G---G----ERFDVLKRMIL 311 685 15384987 218 AFIDGVDFVFLEAPPFRH---R---------HNDIY----G---G----ERFDVLKRMIL 254 686  7489710 313 AFIDGVDFVFIDAPLFRH---R---------QDDIY----G---G----SRQEIMKRMIL 349 687 16265834 391 AFIDGVDFVFIDAPLFRH---R---------QDDIY----G---G----NRQEIMKRMIL 427 688 15232051 373 AFIDGVDFVFIDSPEFRH---L---------SNNIY----G---G----NRLDILKRMVL 409 689  7489695 72 AYIDGVDFVFIDAPLFRH---R---------QEDIY----G---G----SRQEIMKRMIL 108 690  6467503 332 AFIDGVDFVFIDSPMFRH---I---------GNDIY----G---G----NRMDILKRMVL 368 691  2833384 333 TYIDGVDIVFIDSPIFRN---L---------ESNIY----G---G----NRLDILRRMVL 369 692  2129898 333 TYIDGVDIVFIDSPIFRN---L---------ESNIY----G---G----NRLDILRRMVL 369 693  3192881 211 AYIDNVDFVFIDSPIFQH---R---------GNNIY----G---G----NRVDILKRMDL 247 694  8953571 379 AYIDGVDFVFIDAPLFRH---R---------QEDIY----G---G----SRQEIMKRMIL 415 695  7529653 380 AYIDGVDFVFIDAPLFRH---R---------QEDIY----G---G----SRQEIMKRMIL 416 696  8953571 380 AYIDGVDFVFIDAPIFRH---R---------QEDIY----G---G----SRQEIMKRMIL 416 697  5825480 380 AYIDGVDFVFIDAPLFRH---R---------QEDIY----G---G----SRQEIMKRMIL 416 698 14495348 330 AYIDGVDFVFIDNPIFHH---V---------ENDIY----G---G----DRTDILKRMVL 366 699  2833390 368 ALLMDCDFVFIHSHMFRH---I---------GNNIY----G---G----NRVDILKRMVL 404 700  8708896 157 AFVDGVDYVFVDHPTFHG---R---------GKNIY----G---G----ERQEILFRCAL 193 701  5880466 217 EYRDNVDWVFVDHPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 255 702  9369334 217 EYRDNVDWVFVDHPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 255 703 15237934 221 EYRDGVDWVFVDHKSY-H---R---------PGNPY----GDSKG----AFGDNQFRFTL 259 704  7188796 213 EYRDNVDWVFVDHPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 251 705  6103327 217 EYRDNVDWVFVDHPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 255 706  9369336 217 EYRDNVDWVFVDHPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 255 707  6690399 144 EHRDGVDWVFVDHKSY-H---R---------PGNPY----GDSKG----AFGDNQFRFTL 182 708  2829792 210 EYRAGVDWVFVDHSSYCRPGTP---------YGDIY----G---A----FG-DNQFRFTL 248 709  2833387 71 EYRDNVDWVFVDUPSY-H---R---------PGSLY----GDNFG----AFGDNQFRYTL 109 710 12019656 217 EYRDSVDWVFVDHPSY-H---R---------PGNLY----GDKFG----AFGDNQFRYTL 255 711  7489712 210 EYRDSVDWVFVDNPSY-H---R---------PGNLY----GDKFG----AFGDNQFRYTL 248 712  5295947 211 EYRDSVDWVFVDHPSY-H---R---------PGNLY----GDNFG----AFGDNQFRYTL 249 713  1549232 211 EYRDSVDWVFVDNPSY-H---R---------PGNLY----GDNFC----AFGDNQFRYTL 249 714  2833377 211 EYRDSVDWVFVDHPSY-H---R---------PGNLY----GDNFG----AFGDNQFRYTL 249 715  6136121 154 CYKRGVDRVFVDHPIFLE---KVWGKT----KSKIYGPNAG---T----DYQDNQLRFSL 199 716   228210 153 CYKRGVDRVFVDHPMFLE---KVWGKT----GSKIY----G---PKAGLDYLDNELRFSL 198 717   297196 153 CYKRGVDRVFVDHPMFLE---KVWGKT----GSKIY----G---PKAGLDYLDNELRFSL 198 718  2833388 154 SYKRGVDRVFVDHPMFLE---KVWGKT----GSKIY----G---PRAGLDYQDNQLRFSL 199 719 15637079 154 SYKRGVDRVFVDHPMFLE---KVWGKTGSMLYGPKA----G---K----DYKDNQLRFSL 199 720   602594 153 CYKRGVDRVFVDHPMFLE---KVWGKT----GSKIY----G---PKAGLDYLDNELRFSL 198 721  2833381 154 SYKRGVDRVFVDHPMFLE---KVWGKTGSMLYGPKA----G---K----DYKDNQLRFSL 199 722  5441242 152 CYKQGVDRVFVDHPCFLE---KVWGKT----GSKLY----G---PSAGVDYEDNQLRYSL 197 723 15223331 156 CYKRGVDRVFVDHPIFLA---KVVGKTCSKIYGPIT----G---V----DYNDNQLRFSL 201 724 12003285 150 CYKRGVDRVFVDHPLFLE---KVWGKT----KSKVY----G---PSAGVDYEDNQLRFSL 195 725  3832512 153 CYKRGVDRVFVDHPLFLE---KVWGKT----ESKLY----G---PKTGVDYKDNQLRFSL 198 726 15626365 159 CFKRGVDRVFVDHPIFLE---KVWGKTGTKLYGPAA----G---D----DYQDNQLRFSI 204 727  2833383 149 CYKRGVDRVFVDHPLFLE---RVWGKT----GSKLY----G---PKTGIDYRDNQLRFSL 194 728  6624281 149 CYKRGVDRVFVDHPCFLE---KVRGKT----KEKIYGPDAG---T----DYEDNQQRFSL 194 729 17736918 79 CYKRGVDRVFVDHPCFLE---KVRGKT----KEKIYGPDAG---T----DYEDNQQRFSL 124 730  4760584 149 CYKRGVDRVFVDHPCFLE---KVRGKT----KEKIYGPDAG---T----DYEDNQQRFSL 194 731  6492245 144 CYKRGVDRVFVDHPMFLE---KVWGKTGSKLYGPTT----G---T----DFRDNQLRFCL 189 682 MaizeSSIIb 316 FCKAAVEVPWYA-----PCGGTV-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 361 683  7489711 316 FCKAAVEVPWYA-----PCGGTV-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 361 684 15028467 312 FCKAAVEVPWFA-----PCGGSI-----YGDG----NLVFIANDWHTALLPVCLKAYYRD 357 685 15384987 255 FCKAAVEVPWFA-----PCGGSI-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 300 686  7489710 350 FCKVAVEVPWHV-----PCGGVC-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 395 687 16265834 428 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFLANDWHTALLPVYLKAYYRD 473 688 15232051 410 FCKAAVEVPWYV-----PCGGVC-----YGDG----NLAFIANDWHTALLPVYLKAYYRD 455 689  7489695 109 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 154 690  6467503 369 FCKAAVEVPWHV-----PCGGVC-----YGDG----NLAFIANDWHTALLPVYLKAYYRD 414 691  2833384 370 FCKAAVEVPWHV-----PCGGIC-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 415 692  2129898 370 FCKAAVEVPWHV-----PCGGIC-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 415 693  3192881 248 FCKAAIVVPWHV-----PCGGIC-----YGDG----NLVFIANDWHTALLPVYLKAYFRD 293 694  8953573 416 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 461 695  7529653 417 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 462 696  8953571 417 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 462 697  5825480 417 FCKAAVEVPWHV-----PCGGVP-----YGDG----NLVFIANDWHTALLPVYLKAYYRD 462 698 14495348 367 LCKAAIEVPWYV-----PCGGYC-----YGDG----NLVFLANDWHTALLPVYLKAYYHD 412 699  2833390 405 FCKAAIEVPWHV-----PCGGVC-----YGDG----NLVFIANDWHTALLPAYLKAYYRD 450 700  8708896 194 LCKAALEAVWHV-----PCGGIT-----YGDD----NLCFIANDWHTALLPVYLQAHYRD 239 701  5880466 256 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 300 702  9369334 256 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 300 703 15237934 260 LCHAACEAPLVL-----PLGGFT-----YGEK----SL-FLVNDWHAGLVPILLAAKYRP 304 704  7188796 252 LCYAACEAPLIL-----ELGGYI-----YGQ-----SCMFVVNDWHASLVPVLLAAKYRP 296 705  6103327 256 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 300 706  9369336 256 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 300 707  6690399 183 LCHAACEAPLVL-----PLGGFT-----YGEK----SL-FLVNDWHAGLVPILLAAKYRP 227 708  2829792 249 LSHAACEAPLVL-----PLGGFT-----YGEK----CL-FLANDWHAALVPLLLAAKYRP 293 709  2833387 110 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 154 710 12019656 256 LCYAACEAPLVL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 300 711  7489712 249 LCYAACEAPLIL-----ELGGYI-----YGQ-----NCMFVVNDWHASLVPVLLAAKYRP 293 712  5295947 250 LCYAACEAPLIL-----ELGGYI-----YGQ-----KCMFVVNDWHASLVPVLLAAKYRP 294 713  1549232 250 LCYAACEAPLIL-----ELGGYI-----YGQ-----KCMFVVNDWHASLVPVLLAAKYRP 294 714  2833377 250 LCYAACEAPLIL-----ELGGYI-----YGQ-----KCMFVVNDWHASLVPVLLAAKYRP 294 715  6136121 200 LCQAALEAPRVL-----NLTSSK-----YFSGPYGEDVVFVANDWHTALLPCYLKSMYQS 249 716   228210 199 LCQAALEAPKVL-----NLNSSN-----YFSGPYGEDVLFIANDWHTALIPCYLKSMYQS 248 717   297196 199 LCQAALEAPKVL-----NLNSSN-----YFSGPYGEDVLFIANDWHTALIPCYLKSMYQS 248 718  2833388 200 LCLAALEAPRVL-----NLNSSKNFSGPYGE-----EVAFIANDWHTALLPCYLKAIYQP 249 719 15637079 200 LCQAALEAPRVL-----NLNSSN-----YFSGPYGEDVVFVANDWHTALLPCYLKTMYQS 249 720   602594 199 LCQAALEAPKVL-----NLSSSN-----YFSGPYGEDVLFIANDWHTALIPCYLKSMYQS 248 721  2833381 200 LCQAALEAPRVL-----NLNSSK-----YFSGPYGEDVVFVANDWHTALLPCYLKTMYQS 249 722  5441242 198 LCQAALEAPRVL-----NLNSNK-----YFSGPYGEDVIFVANDWHTALLPCYLKSMYQT 247 723 15223331 202 LCQAALEAPQVL-----NLNSSK-----YFSGPYGEDVVFVANDWHTALLPCYLKSMYQS 251 724 12003285 196 LSLAALEAPRVL-----NLTSNK-----YFSGPYGEDVVFVANDWHTAVLPCYLKTIYQP 245 725  3832512 199 LCQAALEAPRVL-----NLNSNK-----HFSGPYGEDVVFVANDWHTALLPCYLKSLYKS 248 726 15626365 205 FCQAALEAARVL-----NLKSNK-----YFSGPYGEDVIFVANDWHTALISCYMKSMYQS 254 727  2833383 195 LCQAALEAPRVL-----NLNSSK-----YFSGPYGEDVIFVANDWHSALIPCYLKSMYKS 244 728  6624281 195 LCQAALEVPRILDLNNNPHFSGP-----YGE-----DVVFVCNDWHTGLLACYLKSNYQS 244 729 17736918 125 LCQAALEVPRIL-----NLDNNP-----YFSGPYGEDVVFVCNDWHTGLLACYLKSNYQS 174 730  4760584 195 LCQAALEVPRIL-----NLDNNP-----YFSGPYGEDVVFVCNDWHTGLLACYLKSNYQS 244 731  6492245 190 LCLAALEAPRVL-----NLNNSE-----YFSGPYGENVVFVANDWHTAVLPCYLKSMYKQ 239 682 MaizeSSIIb 362 NGLMQYARSVLVIHNIAHQGRGPVDDFVNFDLPEHYIDHF--------KLYDN----IG- 408 683  7489711 362 NGLMQYARSVLVIHNIAHQGRGPVDDFVNFDLPEHYIDHF--------KLYDN----IG- 408 684 15028467 358 NGLMQYTRSVLVIHNIAHQGRGPVDDFATMDLPEHYIDHF--------RLYDP----VG- 404 685 15384987 301 NGLMQYTRSVLVIHNIAHQGRGPVDDFATMDLPEHYIDHF--------RLYDP----VG- 347 686  7489710 396 HGLMQYTRSVLVIHNIAHQGRGPVDEFPYMDLPEHYLQRF--------ELYDP----VG- 442 687 16265834 474 NGMMQYTRSVLVIHNIAYQGRGPVDEFPYMELPEHYLDHF--------KLYDP----VG- 520 688 15232051 456 HGIMKYTRSVLVIHNIAHQGRGPVDDFSYVDLPSHYLDSF--------KLYDP----VG- 502 689  7489695 155 HGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYLEHF--------RLYDP----VG- 201 690  6467503 415 NGLMQYTRSVLVIHNIAHQGRGPSGDFSYVGLPEHYIDLF--------KLHDP----IG- 461 691  2833384 416 HGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLDLF--------KMYDP----VG- 462 692  2129898 416 HGLMNYTRSVLVIHNIAHQGRGPVEDFNTVDLSGNYLDLF--------KMYDP----VG- 462 693  3192881 294 NGVMKFTRSVLVIHNIAHQGRGPMDDFSIVDLPAQYADLF--------KLYDP----VG- 340 694  8953573 462 HGLMQYTRSIMVIHNIAHQGRGFVDEFPFTELPEHYLEHF--------RLYDP----VG- 508 695  7529653 463 HGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYLEHF--------RLYDP----VG- 509 696  8953571 463 HGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYLEHF--------RLYDP----VG- 509 697  5825480 463 HGLMQYTRSIMVIHNIAHQGRGPVDEFPFTELPEHYLEHF--------RLYDP----VG- 509 698 14495348 413 NGFMIYARSVLVIHNIAHQGRGPLDDFSYLDLPVDYMDLF--------KLYDP----FG- 459 699  2833390 451 NGIMNYTRSVLVIHNIAHQGRGPLEDFSYVDLPPHYMDPF--------KLYDF----VG- 497 700  8708896 240 YGEMTYARCAFVIHNMAHQGRGPFVESEHLELNEEYRERF--------RLYDP----IG- 286 701  5880466 301 YGVYRDSRSTLVIHNLAHQGLEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 355 702  9369334 301 YGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPFEWYGALEWVFPEWARRHAL----DK- 355 703 15237934 305 YGVYKDARSILIIHNLAHQGVEPAATYTNLGLPSEW--------------YGA----VGW 346 704  7188796 297 YGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 351 705  6103327 301 YGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 355 706  9369336 301 YGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 355 707  6690399 228 YGVYKDARSILIIHNLAHQGVEPAATYTNLGLPSEW--------------YGA----VGW 269 708  2829792 294 YGVYKDARSIVAIHNIAHQGVEPAVTYNNLGLPPQWYGAVEWIFPTWARAHAL----DT- 348 709  2833387 155 YGVYRDSRSTLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 209 710 12019656 301 YGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 355 711  7489712 294 YGVYKDSRSILVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 348 732  7484400 4                   RGRGPFVESEHLELNEEYRERF--------RLYDP----IG- 32 712  5295947 295 YGVYRDARSVLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 349 713  1549232 295 YGVYRDARSVLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 349 714  2833377 295 YGVYRDARSVLVIHNLAHQGVEPASTYPDLGLPPEWYGALEWVFPEWARRHAL----DK- 349 715  6136121 250 KGMYLHAKVAFCIHNIAYQGRFGSSDFCLLNLPDQFKSSF--------DFFDGYEKPVK- 300 716   228210 249 RGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRGSF--------DFIDGYEKPVK- 299 717   297196 249 RGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRGSF--------DFIDGYEKPVK- 299 718  2833388 250 MGIYKHAKVAFCIHNIAYQGRFAFSDFPRLNLPDKFKSSF--------DFIDGYEKPVK- 300 719 15637079 250 RGIYMNAKVAFCIHNIAYQGRFAFSDFSLLNLPDEYKGSF--------DFIDGYDKPVK- 300 720   602594 249 RGIYLNAKVAFCIHNIAYQGRFSFSDFPLLNLPDEFRGSF--------DFIDGYEKPVK- 299 721  2833381 250 RGIYMNAKVAFCIHNIAYQGRFAFSDFSLLNLPDEYKGSF--------DFIDGYDKPVK- 300 722  5441242 248 RGVYRNTKVAFCIHNISYQGRHPFEDFPLLNLPNEYRSAF--------DFTDGHLKPVR- 298 723 15223331 252 RGVYMNAKVVFCIHNIAYQGRFAFDDYSLLNLPISFKSSF--------DFMDGYEKPVK- 302 724 12003285 246 KGIYTNAKVVLCIHNIAYQGRFAFSDFYKLNLPDQLKSSF--------DFMDGYEKPVK- 296 725  3832512 249 KGIYKSAKVAFCIHNIAYQGRHAFSDLSLLNLPNEFRSSF--------DFIDGYDKPVK- 299 726 15626365 255 IGIFRNAKVVFCIHNIAYQGRFAFTDYSLLNLPDQFKSSF--------DFLDGHVKPIV- 305 727  2833383 245 RGLYKNAKVAFCIHNIAYQGRNAFSDFSLLNLPDEFRSSF--------DFIDG----YNK 292 728  6624281 245 NGIYRTAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSF--------DFIDGYDKPVE- 295 729 17736918 175 NGIYRAAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSF--------DFIDGYDKPVE- 225 730  4760584 245 NGIYRAAKVAFCIHNISYQGRFSFDDFAQLNLPDRFKSSF--------DFIDGYDKPVE- 295 731  6492245 240 NGIYVNAKVAFCIHNIAYQGRFPRVDFELLNLPESFMPSF--------DFVDGHVKPVV- 290

[0401] TABLE XXVII Maize soluble starch synthase IIb (SSIIb) “LINKR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                Sequence                end # 733 MaizeSSIIb 409 -------------GDHSNVFAAGLKTADRVVTVSNGYMWELKT-S-EG-GWGLHDIINQN 452 734  7489711@ 409 -------------GDHSNVFAAGLKTADRVVTVSNGYMWELKT-S-EG-GWGLHDIINQN 452 735 15028467@ 405 -------------GEHSNVFAAGLKMADRAVTVSHGYLWEIKT-M-DG-GWGLHEIINHN 448 736 15384987@ 348 -------------GEHSNVFAAGLKMADRAVTVSHGYLWEIKT-M-DG-GWGLHEIINHN 391 737  7489710@ 443 -------------GEHANIFAAGLKMADRVVTVSRGYLWELKT-V-EG-GWGLHDIIRSN 486 738 16265834@ 521 -------------GEHANIFGAGLKMADRVVTVSPGYLWELKT-T-EG-GWGLHDIIREN 564 739 15232051@ 503 -------------GEHFNIFAAGLKAADRVLTVSHGYSWEVKT-L-EG-GWGLHNIINEN 546 740  7489695@ 202 -------------GEHANYFAAGLKMADQVVVVSPGYLWELKT-V-EG-GWGLHDIIRQN 245 741  6467503@ 462 -------------GDHFNIFAPGLKVADRVVTVSHGYAWELKT-S-EG-GWGLHNIINEN 505 742  2833384@ 463 -------------GEHFNIFAAGLKTADRIVTVSHGYAWELKT-S-EG-GWGLHNIINES 506 743  2129898@ 463 -------------GEHFNIFAAGLKTADRIVTVSHGYAWELKT-S-EG-GWGLHNIINES 506 744  2192881@ 341 -------------GDHFNIFAAGLKTADRVVTVSHGYAWELKT-S-EG-GWGLNGIRNEN 384 745  8953573@ 509 -------------GEHANYFAAGLKMADQVVVVSPGYLWELKT-V-EG-GWGLHDIIRQN 552 746  7529653@ 510 -------------GEHANYFAAGLKMADQVVVVSPGYLWELKT-V-EG-GWGLHDIIRQN 553 747  8953571@ 510 -------------GEHANYFAAGLKMADQVVVVSPGYLWELKT-V-EG-GWGLHDIIRQN 553 748  5825480@ 510 -------------GEHANYFAAGLKMADQVVVVSPGYLWELKT-V-EG-GWGLHDIIRQN 553 749 14495348@ 460 -------------GDHLNIFAAGIKAADRLLTVSHGYAWELKT-A-EG-GWGLHGIINES 503 750  2833390@ 498 -------------GEHFNIFAAGLKTADRVVTVSHGYSWELKT-S-QG-GWGLHQIINEN 541 751  8708896@ 287 -------------GEHMNVMKAGLECAHRLVAVSKCYAWECQT-V-EG-GWGLHEVIKVN 330 752  5880466@ 356 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 399 753  9369334@ 356 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 399 754 15237934@ 347 VFPTWARTHALDTGEAVNVLKGAIVTSDRIITVSQGYAWEITT-V-EG-GYGLQDLLSSR 403 755  7188796@ 352 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 395 756  6103327@ 356 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 399 757  9369336@ 356 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 399 758  6690399@ 270 VFPTWARTHALDTGEAVNVLKGAIVTSDRIITVSQGYAWEITT-V-EG-GYGLQDLLSSR 326 759  2829792@ 349 -------------GETVNVLKGAIAVADRILTVSQGYSWEITT-P-EG-GYGLHELLSSR 392 760  2833387@ 210 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 253 761 12019656@ 356 -------------GEAVNFLKGAVVTADRIVTVSKGYSWEVTT-A-EG-GQGLNELLSSR 399 762  7489712@ 349 -------------GEAVNFLKGAVVTADRIVTVSKGYSWEVTT-A-EG-GQGLNELLSSR 392 763  7484400@ 33 -------------GEHMNVMKAGLECAHRLVAVSKCYAWECQT-V-EG-GWGLHEVIKVN 76 764  5295947@ 350 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 393 765  1549232@ 350 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 393 766  2833377@ 350 -------------GEAVNFLKGAVVTADRIVTVSQGYSWEVTT-A-EG-GQGLNELLSSR 393 767  6136121@ 301 -------------GRKINWMKAGILESDRVVTVSPYYAMELVSGA-EK-GVELDNVIAKT 345 768   228210@ 300 -------------GRKINWMKAGILESHRVVTVSPYYAQELVS-AVDK-GVELDSVLRKT 344 769   297196@ 300 -------------GRKINWMKAGILESHRVVTVSPYYAQELVS-AVDK-GVELDSVLRKT 344 770  2833388@ 301 -------------GRKINWMKAGILESDRVLTVSPYYAQEVIS-GVER-GVELDNFIRKT 345 771 15637079@ 301 -------------GRKINWMKAGIREADRVFTVSPNYAKELVS-CVSK-GVELDNHI--R 343 772   602594@ 300 -------------GRKINWMKAGILESHRVVTVSPYYAQELVS-AVDK-GVELDSVLRKT 344 773  2833381@ 301 -------------GRKINWMKAGIREADRVFTVSPNYAKELVS-CVSK-GVELDNHI--R 343 774  5441242@ 299 -------------GRKINWMKAAILESDLVLTVSPYYARELVS-G-EDRGVELDNIIRKT 343 775 15223331@ 303 -------------GRKINWMKAAILEAHRVLTVSPYYAQELIS-GVDR-GVELHKYLRMK 347 776 12003285@ 297 -------------GRKINWMKAGIIESDRVLTVSPYYANELVS-GPDK-GVELDNILRK- 340 777  3832512@ 300 -------------GRKINWMKAGVLESDRVFTVSPYYAKELVS-G-EDRGVELDNIIRS- 343 778 15626365@ 306 -------------GRKINWMKAGIIESHRVLTVSPYYAQELVS-GPDK-GVELDNILRRV 350 779  2833383@ 293 PCE----------GKKINWMKAGILESDQVFTVSPHYAKELIS-G-EDRGVELDNIIRST 340 780  6624281@ 296 -------------GRKINWMKAGILQADKVLTVSPYYAEELIS-G-EARGCGLDNIMRLT 340 781 17736918@ 226 -------------GRKINWMKAGILQADKVLTVSPYYAEELIS-G-ETRGCELDNIMRLT 270 782  4760584@ 296 -------------GRKINWMKAGILQADKVLTVSPYYAEELIS-G-EARGCELDNIMRLT 340 783  6492245@ 291 -------------GRKINWMKAGITECDVVLTVSPHYVKELTS-GPEK-GVELDGVLRAK 335 733 MaizeSSIIb 453 DWKLQGIVNGIDMSEWNPAVD----VHL----HSDDYTN--YTFETLDTGKRQCKAALQR 502 734  7489711@ 453 DWKLQGIVNGIDMSEWNPAVD----VHL----HSDDYTN--YTFETLDTGKRQCKAALQR 502 735 15028467@ 449 DWKLQGIVNGIDMAEWNPEVD----EHL----QSDGYAN--YTFETLDTGKKQCKEALQR 498 736 15384987@ 392 DWKLQGIVNGIDMAEWNPEVD----EHL----QSDGYAN--YTFETLDTGKKQCKEALQR 441 737  7489710@ 487 DWKINGIVNGIDHQEWNPKVD----VHL----RSDGYTN--YSLETLDAGKRQCKAALQR 536 738 16265834@ 565 DWKMNGIVNGIDYREWNPEVD----VHL----QSDGYAN--YTVASLDSSKPRCKAALQR 614 739 15232051@ 547 DWKFRGIVNGIDTQEWNPEFD----TYL----HSDDYTN--YSLENLHIGKPQCKAALQK 596 740  7489695@ 246 DWKTRGIVNGIDNMEWNPEVD----AHL----KSDGYTN--FSLRTLDSGKRQCKEALQR 295 741  6467503@ 506 HWKLQGIVNGIDAKEWNPQFD----IQL----TSDGYTN--YSLETLDTGKPQCKTALQN 555 742  2833384@ 507 DWKFRGIVNGVDTKDWNPQFD----AYL----TSDGYTN--YNLKTLQTGKRQCKAALQR 556 743  2129898@ 507 DWKFRGIVNGVDTKDWNPQFD----AYL----TSDGYTN--YNLKTLQTGKRQCKAALQR 556 744  3192881@ 385 EWKLQGIVNGIDIEEWNPQLD----VYL----KSDGYAE--YSLDTLQTGKPQCKAALQK 434 745  8953573@ 553 DWKTRGIVEGIDNMEWNPEVD----VHL----KSDGYTN--FSLGTLDSGKRQCKEALQR 602 746  7529653@ 554 DWKTRGIVNGIDNMEWNPEVD----AHL----KSDGYTN--FSLRTLDSGKRQCKEALQR 603 747  8953571@ 554 DWKTRGIVNGIDNMEWNPEVD----VHL----QSDGYTN--FSLSTLDSGKRQCKEALQR 603 748  5825480@ 554 DWKTRGIVNGIDNMEWNPEVD----VHL----KSDGYTN--FSLGTLDSGKRQCKEALQR 603 749 14495348@ 504 DWKFQGIVNGIDTTDWNPRCD----IHL----KSDGYTN--YSLETVQAGKQQCKAALQK 553 750  2833390@ 542 DWKLQGIVNGIDTKEWNPELD----VHLP---RSDGYMN--YSLDTLQTGKPQCKAALQK 592 751  8708896@ 331 NWKLRGIVNGIDYKEWNPICD----EFL----TTDGYAH--YDVDTLAEGKAKCKAALQK 380 752  5880466@ 400 KSVLNGIVNGIDINDWNPTTD----KCL----PE----H--YSVDDL-SGKAKCKAELQK 444 753  9369334@ 400 KSVLNGIVNGIDINDWNPTTD----KCL----PH----H--YSVDDL-SGKAKCKAELQK 444 754 15237934@ 404 KSVINGITNGINVDEWNPSTD----EHIPFHYSADDVSE-----------KIKCKMALQK 448 755  7188796@ 396 KSVLNGIVNGIDINDWNPTTD----KCL----PH----H--YSVDDL-SGKAKCKAELQR 440 756  6103327@ 400 KSVLNGIVNGIDINDWNPTTD----KCL----PH----H--YSVDDL-SGKAKCKAELQK 444 757  9369336@ 400 KSVLNGIVNGIDINDWNPTTD----KCL----PH----H--YSVDDL-SGKAKCKAELQK 444 758  6690399@ 327 KSVINGITNGINVDEWNPSTD----EHIPFHYSADDVSE-----------KIKCKMALQK 371 759  2829792@ 393 QSVLNGITNGIDVNDWNPSTD----EHI----AS----H--YSINDL-SGKVQCKTDLQK 437 760  2833387@ 254 KSVLNGIVNGIDINDWNPTTD----KCL----PH----H--YSVDDL-SGKAKCKAELQK 298 761 12019656@ 400 KSVLNGIVNGIDINDWNPATDKCIPCHY----SVDDL-----------SGKAKCKSALQK 444 762  7489712@ 393 KSVLNGIVNGIDINDWNPATDKCIPCHY----SVDDL-----------SGKAKCKGALQK 437 763  7484400@ 77 NWKLRGIVNGIDYKEWNPICD----EFL----TTDGYAH--YDVDTLAEGKAKCKAALQK 126 764  5295947@ 394 KSVLNGIVNGIDINDWNPSTD----KFL----P----YH--YSVDDL-SGKAKCKAELQK 438 765  1549232@ 394 KSVLNGIVNGIDINDWNPSTD----KFL----P----YH--YSVDDL-SGKAKCKAELQK 438 766  2833377@ 394 KSVLNGIVNGIDINDWNPSTD----KFL----P----YH--YSVDDL-SGKAKCKAELQK 438 767  6136121@ 346 --SITGIVNGMDTQEWNPATD----KHI----D----TN--YDITTVMDAKPLLKEALQA 389 768   228210@ 345 --CITGIVNGMDTQEWNPA--------------TDKYTDVKYDITTVMDAKPLLKEALQA 388 769   297196@ 345 --CITGIVNGMDTQEWNPA--------------TDKYTDVKYDITTVMDAKPLLKEALQA 388 770  2833388@ 346 G--IAGIINGMDVQEWNPVTD----KYI----D----IH--YDATTVMDAKPLLKEALQA 389 771 15637079@ 344 DCGITGICNGMDTQEWNPATD----KYL----A----VK--YDITTVEQAKPLLKEALQA 389 772   602594@ 345 --CITGIVNGMDTQEWNPA--------------TDKYTDVKYDITTVMDAKPLLKEALQA 388 773  2833381@ 344 DCGITGICNGMDTQEWNPATD----KYL----A----VK--YDITTVMQAKPLLKEALQA 389 774  5441242@ 344 G--VAGIVNGMDIREWSPKTDKF--IDI----HFDT--------TSVKEAKFLLKEALQA 387 775 15223331@ 348 --TVSGIINGMDVQEWNPSTD----KYI----D----IK--YDITTVTDAKPLIKEALQA 391 776 12003285@ 341 -CTVTGIVNGMDTQEWNPATD----KYI----DN----H--YDITTVMDGKPLLKEALQA 385 777  3832512@ 344 -IGITGIVNGMDNREWSPQTD----RYI----D----VH--YDASTVTEAKAILKEALQA 388 778 15626365@ 351 G--VTGIVNGMDVQEWNPSTD----KYI----S----IK--YDASTVLEGKALLKEELQA 394 779  2833383@ 341 G--IIGIVNGMDNREWSPQTD----RYI----D----VH--YNETTVTEAKPLLKGTLQA 384 780  6624281@ 341 G--ITGIVNGMDVSEWDPIKD----KFL--------TVN--YDVTTALEGKALNKEALQA 384 781 17736918@ 271 G--ITGIVNGMDVSEWDPTKD----KFL----A----VN--YDITTALEGKALNKEALQA 314 782  4760584@ 341 G--ITGIVNGMDVSEWDPTKD----KFL----A----VN--YDITTALEGKALNKEALQA 384 783  6492245@ 336 PLE-TGIVNGMDVVDWNPATD----KYI----S----VK--YNATTVAEARALNKEILQA 380

[0402] TABLE XXVIII Maize soluble starch synthase IIb (SSIIb) “GLYTR” Domain Alignments with other similar Proteins SEQ Accession a.a a.a. Id.No. Number # (start)                 Sequence                 end # 784 MaizeSSIIa 503 QLGLQVRDDVPLIGFIGRLDHQKGVDIIADAIHWI-AG-QDVQLVMLGTGRADLEDMLRR 560 785  7489711 503 QLGLQVRDDVPLIGFIGRLDHQKGVDIIADAIHWI-AG-QDVQLVMLGTGRADLEDMLRR 560 786 15028467 499 QLGLQVRDDVPLIGFIGRLDHQKGVDIIGDAMPWI-AG-QDVQVVMLGTGRPDLEEMLRR 556 787 15384987 442 QLGLQVRDDVPLIGFIGRLDHQKGVDIIGDAMPWI-AG-QDVQVVMLGTGRPDLEEMLRR 499 788  7489710 537 ELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWI-AG-QDVQLVMLGTGRADLERMLQH 594 789 16265834 615 ELGLEVRDDVPLIGFIGRLDGQKGVDIIGDAMPWI-AG-QDVQLVLLGSGRRDLEVMLQR 672 790 15232051 597 ELGLPVRPDVPLIGFIGRLDHQKGVDLIAEAVPWM-MS-QDVQLVMLGTGRPDLEEVLRQ 654 791  7489695 296 ELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLQH 353 792  6467503 556 ELRFAIPPDVPVIGFIGRLDYQKGVDLIAEAIPWM-VG-QDVQLVMLGTGRQDLEEMLRQ 613 793  2833384 557 ELGLPVREDVPIISFIGRLDHQKGVDLIAEAIPWM-MS-HDVQLVMLGTGRADLEQMLKE 614 794  2129898 557 ELGLPVREDVPIISFIGRLDHQKGVDLIAEAIPWM-MS-HDVQLVMLGTGRADLEQMLKE 614 795  3192881 435 EMNLPVRDDVPLIGFIGRLDHQKGVDLIAEAIPWM-MG-QDVQLVMLGTGRPDLEQMLKQ 492 796  8953573 603 ELGLQVRGDVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLEGMLRH 660 797  7529653 604 ELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLQH 661 798  8953571 604 ELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLRH 661 799  5825480 604 ELGLQVRADVPLLGFIGRLDGQKGVEIIADAMPWI-VS-QDVQLVMLGTGRHDLESMLRH 661 800 14495348 554 ELGLPVRGDVPVIAFIGRLDHQKGVDLIAEAMPWI-AG-QDVQLIMLGTGRQDLEDTLRR 611 801  2833390 593 ELGLPVRDDVPLIGFIGRLDPQKGVDLIAEAVPWM-MG-QDVQLVMLGTGRRDLEQMLRQ 650 802  8708896 381 ELGLPVDPDAPMLGFIGRLDYQKGVDLIRDNYDYI-MG-EKCQLVMLGSGRQDLEDALRD 438 803  5880466 445 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMRS 502 804  9369334 445 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMRS 502 805 15237934 449 ELGLPIRPECPMIGFIGRLDYQKGIDLIQTAGPDL-MV-DDIQFVMLGSGDPKYESWMRS 506 806  7188796 441 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPDL-MR-EDVQFVMLGSGDPVFEGWMRS 498 807  6103327 445 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMRS 502 808  9369336 445 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMRS 502 809  6690399 372 ELGLPIRPECPMIGFIGRLDYQKGIDLIQTAGPDL-MV-DDIQFVMLGSGDPKYESWMRS 429 810  2829792 438 ELGLPIRPDCPLIGFIGRLDYQKGVDIILSAIPEL-MQ-NDVQVVMLGSGEKQYEDWMRH 495 811  2833387 299 ELGLPVREDVPLIGFIGRLDYQKGIDLIKMAIPEL-MR-EDVQFVMLGSGDPIFEGWMRS 356 812 12019656 445 ELGLPIRPEVPLIGFIGRLDYQKGIDLIQLIIPHL-MR-DDVQFVMLGSGDPELEDWMRS 502 813  7489712 438 ELGLPIRPDVFLIGFIGRLDYQKGIDLIQLIIPDL-MR-EDVQFVMLGSGDPELEDWMRS 495 814  7484400 127 ELGLPVDPDAPMLGFIGRLDYQKGVDLIRDNYDYI-MG-EKCQLVMLGSGRQDLEDALRD 184 815  5295947 439 ELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMRS 496 816  1549232 439 ELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMRS 496 817  2833377 439 ELGLPIRPDVPLIGFIGRLDYQKGIDLIKLAIPDL-MR-DNIQFVMLGSGDPGFEGWMRS 496 818  6136121 390 AVGLPVDKNIPVIGFIGRLEEQKGSDILVAAISKF-VG-LDVQIIILGTGKKKFEQQIQE 447 819   228210 389 AVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIEQ 446 820   297196 389 AVGLPVDKKIPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIEQ 446 821  2833388 390 EVGLPVDRNVPLIGFIGRLEEQKGSDIFVAAISQL-VE-HNVQIVILGTGKKKFEKQIEH 447 822 15637079 390 AVGLPVDRNIPLIGFIGRLEEQKGSDILYAAISKF-IS-MDVQILILGTGKKKFEQQIEQ 447 823   602594 389 AVGLPVDKKVPLIGFIGRLEEQKGSDILVAAIHKF-IG-LDVQIVVLGTGKKEFEQEIEQ 446 824  2833381 390 AVGLPVDRNIPLIGFIGRLEEQKGSDILYAAISKF-IS-MDVQILILGTGKKKFEQQIEQ 447 825  5441242 388 EVGLPVNRDIPLIGFIGRLEEQKGSDILVEAIPKF-ID-QNVQIIILGTGKKSMEKQIEQ 445 826 15223331 392 AVGLPVDRDVPVIGFIGRLEEQKGSDILVEAISKF-MG-LNVQMVILGTGKKKMEAQILE 449 827 12003285 386 EVGLPVDRNVPLVGFIGRLEEQKGSDILVAALHKF-IE-MDVQVVILGTGKKEFEKQIEQ 443 828  3832512 389 EVGLPVDRNIPVIGFIGRLEEQKGSDILVESIPKF-ID-QNVQIIVLGTGKKIMEKQIEQ 446 829 15626365 395 EVGLPVDKNVPLIAFIGRLEEQKGSDILVEAIPQF-IK-ENVQIVALGTGKKEMEKQLQQ 452 830  2833383 385 EIGLPVDSSIPLIGFIGRLEEQKGSDILVEAIAKF-AD-ENVQIVVLGTGKKIMEKQIEV 442 831  6624281 385 EVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEI-VKEEDVQIVLLGTGKKKFERLLKS 443 832 17736918 315 EVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIVLLGTGKKKFERLLKS 373 833  4760584 385 EVGLPVDRKVPLVAFIGRLEEQKGPDVMIAAIPEILKE-EDVQIVLLGTGKKKFERLLKS 443 834  6492245 381 EVGLPVDSSIPVIVFIGRLEEQKGSDILIAAIPEF-LE-ENVQIIVLGTGKKKMEEELML 438 784 MaizeSSIIb 561 FESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 620 785  7489711 561 FESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 620 786 15028467 557 FESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYSTVPVVHAVGG 616 787 15384987 500 FESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 559 788  7489710 595 LEREHPNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 654 789 16265834 673 FEAQHNSKVRGWVGFSVKMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 732 790 15232051 655 MEHQYRDKARGWVGFSVKTAHRITAGADILLMPSRFEPCGLNQLYAMNYGTIPVVHAVGG 714 791  7489695 354 FEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 413 792  6467503 614 FENQHRDKVRGWVGFSVKTAHRITAGADILLMPSRFEPCGLNQLYAMMYGTIPVVHAVGG 673 793  2833384 615 FEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVGG 674 794  2129898 615 FEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVGG 674 795  3192881 493 IEGQYGDKVRGWVGFSVKTAHRITAGALILLMPSRFEPCGLNQLYAMSYGTVPVVHAVGG 552 796  8953573 661 FEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 720 797  7529653 662 FEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 721 798  8953571 662 FEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 721 799  5825480 662 FEREHHDKVRGWVGFSVRLAHRITAGADALLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 721 800 14495348 612 LESQHYDRVRGWVGFSIRLAHRMTAGADILLMPSRFEPCGLNQLYAMMYGTVPVVHAVGG 671 801  2833390 651 FECQHNDKIRGWVGFSVKTSHRITAGADILLMPSRFEPCALNQLYAMKYGTIPVVHAVGG 710 802  8708896 439 MENRNKNQCRGWVGFSNKMAHRITAAADILLMPSRFEPCGLNQLYAMAYGTVPIVHSVGG 498 803  5880466 503 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 562 804  9369334 503 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 562 805 15237934 507 MEETYRDKFRGWVGFNVPISHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPVVHGTGG 566 806  7188796 499 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 558 807  6103327 503 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 562 808  9369336 503 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 562 809  6690399 430 MEETYRDKFRGWVGFNVPISHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPVVHGTGG 489 810  2829792 496 TENLFKDKFRAWVGFNVPVSHRITAGCDILLMPSRFEPCGLNQLYAMRYGTIPIVHSTGG 555 811  2833387 357 TESSYKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 416 812 12019656 503 TESDFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGG 562 813  7489712 496 TESIFKDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGG 555 814  7484400 185 MENRNKNQCRGWVGFSNKMAHRITAAADILLMPSRFEPCGLNQLYAMAYGTVPIVHSVGG 244 815  5295947 497 TESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 556 816  1549232 497 TESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 556 817  2833377 497 TESGYRDKFRGWVGFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHGTGG 556 818  6136121 448 LEVLYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTIPICASTGG 507 819   228210 447 LEVLYPGKVKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGG 506 820   297196 447 LEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGG 506 821  2833388 448 LEVLYPDKARGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPIVASTGG 507 822 15637079 448 LEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHAMRYGTPCICASTGG 507 823   602594 447 LEVLYPNKAKGVAKFNVPLAHMITAGADFMLVPSRFEPCGLIQLHAMRYGTVPICASTGG 506 824  2833381 448 LEVMYPDKARGVAKFNVPLAHMITAGADFMLIPSRFEPCGLIQLHAMRYGTPCICASTGG 507 825  5441242 446 LEEIYPEKARGIAKFDGPLAHKIIAGSDFIMIPSRFEPCGLVQLHSMPYGTVPIVSSTGG 505 826 15223331 450 LEEKFPGKAVGVAKFNVPLATMITAGADFIIVPSRFEPCGLIQLHAMRYGTVPIVASTGG 509 827 12003285 444 LEELYPGKAVGVAKFNVPLAHKITAGADFMLVPSRFEPCGLIQLHAMRYGTIPICASTGG 503 828  3832512 447 LEVTYPGKAIGVAKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTGG 506 829 15626365 453 LEISYPDKARGVAKFNVPLAHMMIAGADFILIPSRFEPCGLIQLQAMRYGTVPIVASTGG 512 830  2833383 443 LEEKYPGKAIGITKFNSPLAHKIIAGADFIVIPSRFEPCGLVQLHAMPYGTVPIVSSTGG 502 831  6624281 444 VEEKFPTKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGG 503 832 17736918 374 IEEKFPSKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGG 433 833  4760584 444 IEEKFPSKVRAVVRFNAPLAHQMMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGG 503 834  6492245 439 LEAKYPQNARGIAKFNVPLAHMMFAGANFIIVPSRFEPCGLIQLQGMRYGVIPICSSTGG 498 784 MaizeSSIIb 621 LRDTV---------AP-FDPF----NDT---GL----G---W--------TFDR---AEA 645 785  7489711 621 LRDTV---------AP-FDPF----NDT---GL----G---W--------TFDR---AEA 645 786 15028467 617 LRDTV---------AP-FDPF----ADT---GL----G---W--------TFDR---AEA 641 787 15384987 560 LRDTV---------AP-FDPF----ADT---GL----G---W--------TFDR---AEA 584 788  7489710 655 LRDTV---------AP-FDPF----GDA---GL----G---W--------TFDR---AEA 679 789 16265834 733 LRDTM---------SA-FDPF----EDT---GL----G---W--------TFDR---AEP 757 790 15232051 715 LRDTV---------QQ-FDPY----SET---GL----G---W--------TFDS---AEA 739 791  7489695 414 LRDTV---------PP-FDPF----NHS---GL----G---W--------TFDR---AEA 438 792  6467503 674 LRDTV---------QP-FDPF----NES---GL----G---W--------TFDS---AES 698 793  2833384 675 LRDTV---------QP-FNPF----DES---GV----G---W--------TFDR---AEA 699 794  2129898 675 LRDTV---------QP-FNPF----DES---GV----G---W--------TFDR---AEA 699 795  3192881 553 LRDTV---------QP-FDPF----NES---GY----G---W--------TFGR---AEA 577 796  8953573 721 LRDTV---------PP-FDPF----NHS---GL----G---W--------TFDR---AEA 745 797  7529653 722 LRDTV---------PP-FDPF----NHS---GL----G---W--------TFDR---AEA 746 798  8953571 722 LRDTV---------PP-FDPF----NHS---GL----G---W--------TFDR---AEA 746 799  5825480 722 VRDTV---------PP-FDPF----NHS---GL----G---W--------TFDR---AEA 746 800 14495348 672 LRDTV---------EH-YNPY----EES---GL----G---W--------TFEK---AEA 696 801  2833390 711 LRDTV---------QP-FDPL----MSQ---DW----G---G--------PSDR---AEA 735 802  8708896 499 LRDTV---------KQ-YSPF----ENV---GT----G---W--------VFER---AEA 523 803  5880466 563 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSP---LTV 590 804  9369334 563 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSF---LTV 590 805 15237934 567 LRDTV---------EN-FNPYAEGGAGT---GT----G---W--------VFTP---LSK 595 806  7188796 559 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSP---LTV 586 807  6103327 563 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSP---LTV 590 808  9369336 563 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSP---LTV 590 809  6690399 490 LRDTV---------EN-FNPYAEGGAGA---GT----G---W--------VFTP---LSK 518 810  2829792 556 LRDTV---------KD-FNPY----AQE---GIGEGTG---W--------TFSP---LTS 584 811  2833387 417 LRDTV---------ET-FNPFGAK-GEE---GT----G---W--------AFSP---LTV 444 812 12019656 563 LRDTV---------EN-FNPF----GENGEQGT----G---W--------AFAP---LTT 590 813  7489712 556 LRDTV---------EN-FNPF----GENGEQGT----G---W--------AFAP---LTT 583 814  7484400 245 LRDTV---------KQ-YSPF----ENV---GT----G---W--------VFER---AEA 269 815  5295947 557 LRDTV---------EN-FNPFAEK-GEQ---GT----G---W--------AF 579 816  1549232 557 LRDTV---------EN-FNPFAEK-GEQ---GT----G---W--------AF 579 817  2833377 557 LRDTV---------EN-FNPFAEK-GEQ---GT----G---W--------AF 579 818  6136121 508 LVDTV---------TEGFTGF----HMG---AF----NVECA--------TVDP---ADV 536 819   228210 507 LVDTV---------K---EGY----TGF---HM----G---AFNVECD--VVDP---ADV 535 820   297196 507 LVDTV---------K---EGY----TGF---HM----G---AFNVECD--VVDP---ADV 535 821  2833388 508 LVDTV---------KEGYTGF----QMG---AL----H---V--------ECDKIDSADV 536 822 15637079 508 LVDTV---------K---EGY----TGF---HM----G---AFNVDCE--TVDP---EDV 536 823   602594 507 LVDTV---------K---EGY----TGF---HM----G---AFNVECD--VVDP---ADV 535 824  2833381 508 LVDTV---------K---EGY----TGF---HM----G---AFNVDCE--TVDP---EDV 536 825  5441242 506 LVDTV---------Q---EGF----TGF---HM----G---AFNVDCE--AIDP---ADV 534 826 15223331 510 LVDTV---------K---DGY----TGF---HI----G---RFNVKCE--VVDP---DDV 538 827 12003285 504 LVDTV---------K---EGF----TGF---HM----G---AFNVECD--AVDP---ADV 532 828  3832512 507 LVDTV---------KEGYTGF----HVG---AF----SVECE--------AVDP---ADV 535 829 15626365 513 LVDTV---------K---EGF----TGF---HM----G---SFNVKCD--AVDP---VDV 541 830  2833383 503 LVDTVKEGYTGFHAGP-FDVE----CE-----------------------DVDP---DDV 531 831  6824281 504 LVDTI---------VE---------GKT---GF----H---MGRLSVDCNVVEP---ADV 532 832 17736918 434 LVDTI---------VE---------GKT---GF----H---MGRLSVDCNVVEP---ADV 462 833  4760584 504 LVDTI---------VE---------GKT---GF----H---MGRLSVDCNVVEP---ADV 532 834  6492245 499 LVDTV---------SEGVTGF----HMG---SF----N---V--------EFET---VDP 524

[0403] TABLE XXIX Maize soluble starch synthase IIb (SSIIb) “CTEND” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                    Sequence                    end # 835 MaizeSSIIb 646 NRMIDALSHCLTTY--RN--YKE-SWRACRARGMAEDLSWDHAAVLYEDVLVKAKYQW 698 836  7489711 646 NRMIDALSHCLTTY--RN--YKE-SWRACRARGMAEDLSNDHAAVLYEDVLVKAKYQW 698 837 15028467 642 NRMIDALGHCLNTY--RN--YKE-SWRGLQARGMAQDLSWDRAAELYEDVLVKAKYQW 694 838 15384987 585 NRMIDALGHCLNTY--RN--YKE-SWRGLQARGMAQDLSWDHAAELYEDVLVKAKYQW 637 839  7489710 680 NKLIEALRHCLDTY--RK--YGE-SWKSLQARGMSQDLSWDHAAELYEDVLVKAKYQW 732 840 16265834 758 HKLIEALGHCLETY--RK--YKE-SWRGLQVRGMSQDLSWDHAAELYEEVLVKAKYQW 810 841 15232051 740 GKLIHALGNCLLTY--RE--YKE-SWEGLQRRGMTQDLSWDNAAEKYEEVLVAAKYHW 792 842  7489695 439 HKLIEALGHCLRTY--RD--FKE-SWRALQERGMSQDFSWEHAAKLYEDVLVKAKYQW 491 843  6467503 699 HKLIHALGNCLLTY--RE--YKK-SWEGLQRRGMTPNLSWDHAAEKYEETLVAAKYQW 751 844  2833384 700 NKLMAALWNCLLTY--KD--YKK-SWEGIQERGMSQDLSWDNAAQQYEEVLVAAKYQW 752 845  2129898 700 NKLMAALWNCLLTY--KD--YKK-SWEGIQERGMSQDLSWDNAAQQYEEVLVAAKYQW 752 846  3192881 578 NQLIDALGNCLLTY--RQ--YKQ-SWEGLQRRGMMQDLSWDHAAEKYEEVLVAAKYQW 630 847  8953573 746 QKLIEALGHCLRTY--RD--YKE-SWRGLQERGMSQDFSWEHAAKLYEDVLVKAKYQW 798 848  7529653 747 HKLIEALGHCLRTY--RD--FKE-SWRALQERGMSQDFSWEHAAKLYEDVLVKAKYQW 799 849  8953571 747 HKLIEALGHCLRTY--RD--YKE-SWRGLQERGMSQDFSWEHAAKLYEDVLLKAKYQW 799 850  5825480 747 HKLIEALGHCLRTY--RD--YKE-SWRGLQERGMSQDFSWEHAAKLYEDVLLKAKYQW 799 851 14495348 697 NRLIDALGHCLNTY--RN--YRT-SWEGLQKRGMMQDLSWDNAAKLYEEVLLAAKYQW 749 852  2833390 736 SQLIPRIRNCLLTY--RE--YKK-SWEGIQTRCMTQDLSWDNAAQNYEEVLIAAKYQW 788 853  8708896 524 NKLRESINNALYTY--RQ--FRD-SFRGIQRRGMEQDLTWDNAASIYEEVLVAAKYQW 576 854  5880466 591 DKMLWALRTAMSTF--RE--HKP-SWEGLMKRGMTKDHTWDHAAEQYEQI 635 855  9369334 591 DKMLWALRTAMSTF--RE--HKP-SWEGLMKRGMTKDHTWDHAAEQYEQI 635 856 15237934 596 DSMVSALRLAAATY--RE--YKQ-SWEGLMRRGMTRNYSWENAAVQYEQV-----FQW 643 857  7188796 587 EKMLWALRTAISTF--RE--HKP-SWEGLMKRGMTKDHTWDHAAEQYEQI 631 858  6103327 591 DKMLWALRTAMSTF--RE--HKP-SWEGLMKRGMTKDHTWDHAAEQYEQI 635 859  9369336 591 DKMLWALRTANSTF--RE--HKP-SWEGLMKRGMTKDHTWDRAAEQYEQI 635 860  6690399 519 DSMVSALRLAAATY--RE--YKQ-SWEGLMRRGMTRNYSWENAAVQYEQV-----FQW 566 861  2829792 585 EKLLDTLKLAIGTY--TE--HKS-SWEGLMRRGMGRDYSWENAAIQYEQVFTWA 633 862  2833387 445 DKMLWALRTAMSTF--RE--HKP-SWEGLMKRGMTKDHTWDHA 482 863 12019656 591 ENMFVDIANC 600 864  7489712 584 ENMFVDIANC 593 865  7484400 270 NKLRESINNALYTY--RQ--FRD-SFRGIQRRGMEQDLTWDNAASIYEEVLVAAKYQW 322 866  6136121 537 QKIATTVERALAAY--GSVAYKE-MIQNC----MAQDLSWKGPAKNWEKMLL 581 867   228210 536 LKIVTTVAPALAVY--GTLAFAE-MIKNC----MSEELSWKEPAKKWETLLL 580 868   267196 536 LKIVTTVARALAVY--GTLAFAE-MIKNC----MSEELSWKEPAKKWETLLL 580 869  2833388 537 AAIVKTVAPALGTY--AT----A-ALREMILNCMAQDLSWKGPARMWEKMLL 581 870 15637079 537 LKVITTVGRALAMY--GTLAFTE-MIKNC----MSQELSWKGPAKNWETVLL 581 871   602594 536 LKIVTTVARALAVY--GTLAFAE-MIKNC----MSEELSWKEPAKKWETLLL 580 872  2833381 537 LKVITTVGRALAIY--GTLAFTE-MIKNC----MSQELSWKGPAKNWETVLL 581 873  5441242 535 EKIATTVRRALGTY--GT--V---AMEKIIQNCMAQDFSWKGPAKQWEKVL 578 874 15223331 539 IATAKPNTRAVAVYGTSA--MQE-MVKNC----MDQDFSWKGPARLWEKVLL 583 875 12003285 533 LKIVKTVGRALEVY--GTPAFRE-MINNC----MSLDLSWKGPAKNWETVLL 577 876  3832512 536 EKLATTVNRALKTYGTQA--LKE-MILNC----MAQDFSWKGPAKQWEQALL 580 877 15626365 542 DAIPKTVTKALGVYGTSA--FAE-MIKNC----MAQELSWKGPAKKWEEVLL 586 878  2833383 532 DKLAATVKRALKTY--GT----Q-AMKQIILNCMAQNFSWKKPAKLWEKALL 576 879  6624281 533 KKVVTTLKRAVKVV--GTPAYHE-MVKNC----MIQDLSWKGPAKNWEDVLLE 578 880 17736918 463 KKVVTTLKRAVKVV--GTPAYHE-MVKNC----MIQDLSWKGPAKNWEDVLLE 508 881  4760584 533 KKVVTTLKRAVKVV--GTPAYHE-MVKNC----MIQDLSWKGPAKNWEDVLLE 578 882  6492245 525 ADVAAVASNVTRAL--KQ--YKTPSFHAMVQNCMAQDLSWKGPAKKWEEALL 572

[0404] TABLE XXX Identities of the Accession Numbers used in Tables. XXV-XXIX. Accession Brief Description of sequences score Id. producing significant alignments (bits) E−value gi|7489711|pir||T01209 ADPglucose - starch glucosyltransfera . . . 1240 0.0 h gi|15028467|gb|AAK81729.1|AF395537_1 (AF395537) soluble sta . . . 972 0.0 gi|15384987|emb|CAC59826.1| (AJ308110) soluble starch synth . . . 968 0.0 gi|7489710|pir||T01208 ADPglucose - starch glucosyltransfera . . . 869 0.0 gi|16265834|gb|AAL16661.1|AF419099_1 (AF419099) putative so . . . 847 0.0 gi|15232051|ref|NP_186767.1| (NM_110984) putative glycogen . . . 837 0.0 gi|7489695|pir||T06798 probable starch synthase (EC 2.4.1.— . . . 833 0.0 gi|6467503|gb|AAF13168.1|AF173900_1 (AF173900) granule boun . . . 832 0.0 gi|2833384|sp|Q43093|UGS3_PEA Glycogen [starch] synthase, c . . . 832 0.0 gi|2129898|pir||S61505 UDPglucose - starch glucosyltransfera . . . 831 0.0 gi|3192881|gb|AAC19119.1| (AF068834) starch synthase [Ipomo . . . 823 0.0 gi|8953573|emb|CAB96627.1| (AJ269504) starch synthase IIa-3 . . . 814 0.0 gi|7529653|emb|CAB86618.1| (AJ269502) starch synthase IIa-1 . . . 812 0.0 gi|8953571|emb|CAB96626.1| (AJ269503) starch synthase IIa-2 . . . 811 0.0 gi|5825480|gb|AAD53263.1|AF155217_1 (AF155217) starch synth . . . 809 0.0 gi|14495348|gb|AAK64284.1|AF383878_1 (AF383878) soluble sta . . . 802 0.0 gi|2833390|sp|Q43847|UGS3_SOLTU Glycogen [starch] synthase, . . . 785 0.0 gi|8708896|gb|AAC17970.2| (AF026421) soluble starch synthas . . . 669 0.0 gi|5880466|gb|AAD54661.1| (AF091803) starch synthase I [Tri . . . 456 e−127 gi|9369334|emb|CAB99209.1| (AJ292521) starch synthase I-1 [. . . 456 e−127 gi|15237934|ref|NP_197818.1| (NM_122336) soluble starch syn . . . 455 e−127 gi|7188796|gb|AAF37876.1|AF234163_1 (AF234163) starch synth . . . 454 e−126 gi|6103327|gb|AAF03557.1| (AF091802) starch synthase I [Aeg . . . 454 e−126 gi|9369336|emb|CAB99210.1| (AJ292522) starch synthase I-2 [. . . 454 e−126 gi|6690399|gb|AAF24126.1|AF121673_1 (AF121673) soluble star . . . 453 e−126 gi|2829792|sp|P93568|UGS2_SOLTU Soluble glycogen [starch] s . . . 449 e−125 gi|2833387|sp|Q43654|UGS2_WHEAT Soluble glycogen [starch] s . . . 448 e−125 gi|12019656|gb|AAD45815.2| (AF168786) soluble starch syntha . . . 423 e−117 gi|7489712|pir||T01414 ADPglucose - starch glucosyltransfera . . . 422 e−117 gi|7484400|pir||T07924 probable starch synthase (EC 2.4.1.— . . . 413 e−114 gi|5295947|dbj|BAA81848.1| (AB026295) ESTs AU075322(C11109) . . . 412 e−114 gi|1549232|dbj|BAA07396.1| (D38221) SSS1 [Oryza sativa] >gi . . . 412 e−114 gi|2833377|sp|Q40739|UGS2_QRYSA Soluble glycogen [starch] s . . . 411 e−113 gi|6136121|sp|O82627|UGST_ANTMA Granule-bound glycogen [sta . . . 346 4e−94 gi|228210|prf||1718316A granule-bound starch synthase [Sola . . . 327 2e−88 gi|267196|sp|Q00775|UGST_SOLTU Granule-bound glycogen [star . . . 327 3e−88 gi|2833388|sp|Q43784|UGST_MANES Granule-bound glycogen [sta . . . 327 3e−88 gi|15637079|dbj|BAB68126.1| (AB071604) granule-bound starch . . . 326 5e−88 gi|602594|emb|CAA58220.1| (X83220) starch (bacterial glycog . . . 326 6e−88 gi|2833381|sp|Q42857|UGST_IPOBA Granule-bound glycogen [sta . . . 320 2e−86 gi|5441242|dbj|BAA82346.1| (AB029546) granule-bound starch . . . 318 9e−86 gi|15223331|ref|NP_174566.1| (NM_103023) starch synthase, p . . . 318 1e−85 gi|12003285|gb|AAG43519.1|AF210699_1 (AF210699) granule-bou . . . 316 6e−85 gi|3832512|gb|AAC70779.1| (AF097922) granule-bound glycogen . . . 314 2e−84 gi|15626365|emb|CAC69955.1| (AJ345045) granule-bound starch . . . 313 3e−84 gi|2833383|sp|Q43092|UGST_PEA Granule-bound glycogen [starc . . . 312 1e−83 gi|6624281|dbj|BAA88509.1| (AB029061) starch synthase (GBSS . . . 311 1e−83 gi|17736918|gb|AAL41028.1| (AF250137) mutant granule bound . . . 311 2e−83 gi|4760584|dbj|BAA77352.1| (AB019624) starch synthase (GBSS . . . 311 2e−83 gi|6492245|gb|AAF14233.1|AF109395_1 (AF109395) granule-boun . . . 309 5e−83 gi|6624285|dbj|BAA88511.1| (AB029063) starch synthase (GBSS . . . 308 1e−82 gi|11037536|gb|AAG27624.1|AF286320_1 (AF286320) granule bou . . . 308 1e−82 gi|4760582|dbj|BAA77351.1| (AB019623) starch synthase (GBSS . . . 308 1e−82 gi|6318540|gb|AAF06937.1|AF110374_1 (AF110374) granule-boun . . . 308 1e−82 gi|6318538|gb|AAF06936.1|AF110373_1 (AF110373) granule-boun . . . 307 2e−82 gi|6624287|dbj|BAA88512.1| (AB029064) starch synthase (GBSS . . . 306 3e−82 gi|18652407|gb|AAL77109.1|AF474373_6 (AF474373) granule-bou . . . 306 3e−82 gi|136755|sp|P09842|UGST_HORVU Granule-bound glycogen [star . . . 306 4e−82 gi|18139611|gb|AAL58572.1| (AY069940) granule binding starc . . . 305 8e−82 gi|4760580|dbj|BAA77350.1| (AB019622) starch synthase (GBSS . . . 305 1e−81 gi|4588609|gb|AAD26156.1|AF113844_1 (AF113844) granule-boun . . . 305 2e−81 gi|136765|sp|P27736|UGST_WHEAT Granule-bound glycogen [star . . . 304 2e−81 gi|6624283|dbj|BAA88510.1| (AB029062) starch synthase (GBSS . . . 303 3e−81 gi|16716335|gb|AAC17969.3| (AF026420) granule-bound starch . . . 300 3e−80 gi|82478|pir||JQ0703 UDPglucose - starch glucosyltransferase . . . 299 6e−80 gi|2833385|sp|Q43134|UGST_SORBI Granule-bound glycogen [sta . . . 298 1e−79 gi|15900991|ref|NP_345595.1| (NC_003028) glycogen synthase . . . 298 1e−79 gi|15903076|ref|NP_358626.1| (NC_003098) Glycogen synthase . . . 298 2e−79 gi|2833382|sp|Q42968|UGST_ORYGL Granule-bound glycogen [sta . . . 297 2e−79 gi|297424|emb|CAA46294.1| (X65183) glycogen (starch) syntha . . . 296 3e−79 gi|136758|sp|P19395|UGST_ORYSA Granule-bound glycogen [star . . . 296 5e−79 gi|7798551|gb|AAC61675.2| (AF031162) granule-bound starch s . . . 296 5e−79 gi|297422|emb|CAA45472.1| (X64108) starch granule-bound sta . . . 292 1e−77 gi|4588607|gb|AAD26155.1|AF113843_1 (AF113843) granule-boun . . . 289 9e−77 gi|136757|sp|P04713|UGST_MAIZE Granule-bound glycogen [star . . . 288 1e−76 gi|15643657|ref|NP_228703.1| (NC_000853) glycogen synthase . . . 285 9e−76 gi|16080147|ref|NP_390973.1| (NC_000964) starch (bacterial . . . 276 7e−73 gi|15672681|ref|NP_266855.1| (NC_002662) glycogen synthase . . . 273 6e−72 gi|17366711|sp|Q9CHM9|GLGA_LACLA Glycogen synthase (Starch . . . 273 6e−72 gi|2811062|sp|O08328|GLGA_BACST Glycogen synthase (Starch [. . . 267 2e−70 gi|18309046|ref|NP_560980.1| (NC_003366) glycogen synthase . . . 264 2e−69 gi|15613648|ref|NP_241951.1| (NC_002570) starch (bacterial . . . 258 1e−67 gi|15895507|ref|NP_348856.1| (NC_003030) Glycogen synthase, . . . 255 1e−66 gi|17229371|ref|NP_485919.1| (NC_003272) glycogen synthase . . . 246 6e−64 gi|15641730|ref|NP_231362.1| (NC_002505) glycogen synthase . . . 236 6e−61 gi|15620537|gb|AAL03921.1|U30252_9 (U30252) GlgA [Synechoco . . . 235 1e−60 gi|16331219|ref|NP_441947.1| (NC_000911) glycogen synthase . . . 235 1e−60 gi|16766821|ref|NP_462436.1| (NC_003197) glycogen synthase . . . 229 7e−59 gi|16762766|ref|NP_458383.1| (NC_003198) glycogen synthase . . . 228 2e−58 gi|4582783|emb|CAB40375.1| (AJ006752) starch synthase, isof . . . 226 4e−58 gi|17938870|ref|NP_535658.1| (NC_003306) glycogen synthase . . . 225 2e−57 gi|16119514|ref|NP_396220.1| (NC_003064) AGR_pAT_410p [Agro . . . 224 2e−57 gi|16124067|ref|NP_407380.1| (NC_003143) glycogen synthase . . . 223 6e−57 gi|15717885|gb|AAK97773.1| (AY044844) starch synthase isofo . . . 222 1e−56 gi|15803938|ref|NP_289974.1| (NC_002655) glycogen synthase . . . 220 3e−56 gi|15890897|ref|NP_356569.1| (NC_003063) AGR_L_1562p [Agrob . . . 219 9e−56 gi|15236819|ref|NP_193558.1| (NM_117934) starch synthase-li . . . 216 8e−55 gi|17227527|ref|NP_484075.1| (NC_003272) glycogen (starch) . . . 215 1e−54 gi|13476305|ref|NP_107875.1| (NC_002678) glycogen synthase . . . 214 3e−54 gi|6116748|dbj|BAA85761.1| (AB028026) granule-bound starch . . . 213 6e−54 gi|16329217|ref|NP_439945.1| (NC_000911) glycogen (starch) . . . 212 1e−53 gi|9587321|gb|AAF89262.1|AF285987_1 (AF285987) granule-boun . . . 211 2e−53 gi|15602409|ref|NP_245481.1| (NC_002663) GlgA [Pasteurella . . . 211 2e−53 gi|9587293|gb|AAF89248.1|AF285973_1 (AF285973) granule-boun . . . 211 2e−53 gi|14279432|gb|AAK58596.1|AF268969_2 (AF268969) glycogen sy . . . 211 3e−53 gi|7489826|pir||T01265 starch synthase DULL1 - maize >gi|30 . . . 210 5e−53 gi|17366749|sp|Q9EUT5|GLGA_RHITR Glycogen synthase (Starch . . . 209 6e−53 gi|4582789|emb|CAB40374.1| (AJ225088) Starch synthase isofo . . . 209 1e−52 gi|15966599|ref|NP_386952.1| (NC_003047) PROBABLE GLYCOGEN . . . 208 2e−52 gi|9587317|gb|AAF89260.1|AF285985_1 (AF285985) granule-boun . . . 207 2e−52 gi|15606118|ref|NP_213495.1| (NC_000918) glycogen synthase . . . 207 4e−52 gi|9587301|gb|AAF89252.1|AF285977_1 (AF285977) granule-boun . . . 206 5e−52 gi|146139|gb|AAA23870.1| (J02616) glycogen synthase (EC 2.4 . . . 206 7e−52 gi|15221083|ref|NP_172637.1| (NM_101044) putative glycogen . . . 205 2e−51 gi|18461221|dbj|BAB84418.1| (AP003292) putative starch synt . . . 204 2e−51 gi|9587329|gb|AAF89266.1|AF285991_1 (AF285991) granule-boun . . . 203 6e−51 gi|16265159|ref|NP_437951.1| (NC_003078) putative glycogen . . . 202 9e−51 gi|9587352|gb|AAF89276.1|AF286003_1 (AF286003) granule-boun . . . 202 1e−50 gi|7489274|pir||T07663 soluble starch synthase (EC 2.4.1.—) . . . 201 3e−50 gi|9587309|gb|AAF89256.1|AF285981_1 (AF285981) granule-boun . . . 200 4e−50 gi|17548463|ref|NP_521803.1| (NC_003296) PROBABLE GLYCOGEN . . . 200 5e−50 gi|9587343|gb|AAF89273.1|AF285998_1 (AF285998) granule-boun . . . 200 5e−50 gi|9587311|gb|AAF89257.1|AF285982_1 (AF285982) granule-boun . . . 199 6e−50 gi|2833389|sp|Q43846|UGS4_SOLTU Soluble glycogen [starch] s . . . 199 1e−49 gi|17646328|gb|AAL40942.1|AF432915_1 (AF432915) putative st . . . 198 1e−49 gi|9587337|gb|AAF89270.1|AF285995_1 (AF285995) granule-boun . . . 198 2e−49 gi|9587341|gb|AAF89272.1|AF285997_1 (AF285997) granule-boun . . . 197 3e−49 gi|9587305|gb|AAF89254.1|AF285979_1 (AF285979) granule-boun . . . 197 3e−49 gi|16273270|ref|NP_439511.1| (NC_000907) glycogen synthase . . . 197 4e−49 gi|9587348|gb|AAF89274.1| (AF286001) granule-bound starch s . . . 197 4e−49 gi|9587319|gb|AAF89261.1|AF285986_1 (AF285986) granule-boun . . . 196 6e−49 gi|8901183|gb|AAC17971.2| (AF026422) soluble starch synthas . . . 195 1e−48 gi|9587307|gb|AAF89255.1|AF285980_1 (AF285980) granule-boun . . . 194 2e−48 gi|9587323|gb|AAF89263.1|AF285988_1 (AF285988) granule-boun . . . 194 2e−48 gi|9587313|gb|AAF89258.1|AF285983_1 (AF285983) granule-boun . . . 193 6e−48 gi|9587299|gb|AAF89251.1|AF285976_1 (AF285976) granule-boun . . . 191 2e−47 gi|9587327|gb|AAF89265.1|AF285990_1 (AF285990) granule-boun . . . 191 2e−47 gi|9587325|gb|AAF89264.1|AF285989_1 (AF285989) granule-boun . . . 190 4e−47 gi|9587297|gb|AAF89250.1|AF285975_1 (AF285975) granule-boun . . . 190 5e−47 gi|17367070|sp|Q9RNH6|GLGA_RHOSH Glycogen synthase (Starch . . . 190 5e−47 gi|5834407|gb|AAD53959.1|AF181035_3 (AF181035) glycogen syn . . . 190 5e−47 gi|9587295|gb|AAF89249.1|AF285974_1 (AF285974) granule-boun . . . 188 2e−46 gi|9587333|gb|AAF89268.1|AF285993_1 (AF285993) granule-boun . . . 187 3e−46 gi|9502145|gb|AAF88000.1| (AF258609) starch synthase III [A . . . 187 4e−46 gi|15597361|ref|NP_250855.1| (NC_002516) probable glycogen . . . 186 6e−46 gi|9587339|gb|AAF89271.1|AF285996_1 (AF285996) granule-boun . . . 186 7e−46 gi|9502143|gb|AAF87999.1|AF258608_1 (AF258608) starch synth . . . 186 7e−46 gi|9587303|gb|AAF89253.1|AF285978_1 (AF285978) granule-boun . . . 186 7e−46 gi|9587335|gb|AAF89269.1|AF285994_1 (AF285994) granule-boun . . . 185 2e−45 gi|9587331|gb|AAF89267.1|AF285992_1 (AF285992) granule-boun . . . 182 9e−45 gi|17366350|sp|P58395|GLGA_THECA Glycogen synthase (Starch . . . 180 4e−44 gi|15805621|ref|NP_294317.1| (NC_001263) glycogen synthase . . . 180 5e−44 gi|15983795|gb|AAL10494.1| (AY056803) Atlg32900/F9L11_8 [Ar . . . 179 9e−44 gi|17367076|sp|Q9RWS1|GLGA_DEIRA Glycogen synthase (Starch . . . 177 5e−43 gi|15605532|ref|NP_220318.1| (NC_000117) Glycogen Synthase . . . 170 6e−41 gi|3493107|gb|AAD03011.1| (AF079291) granule-bound starch s . . . 167 4e−40 gi|3493007|gb|AAD02961.1| (AF079241) granule-bound starch s . . . 166 6e−40 gi|3493103|gb|AAD03009.1| (AF079289) granule-bound starch s . . . 166 6e−40 gi|7484399|pir|T07926 probable starch synthase (EC 2.4.1.— . . . 165 1e−39 gi|12278417|gb|AAG48949.1| (AY010962) granule-bound starch . . . 164 2e−39 gi|3493005|gb|AAD02960.1| (AF079240) granule-bound starch s . . . 164 2e−39 gi|3493111|gb|AAD03013.1| (AF079293) granule-bound starch s . . . 164 3e−39 gi|15834801|ref|NP_296560.1| (NC_002620) glycogen synthase . . . 164 3e−39 gi|12278503|gb|AAG48992.1| (AY011005) granule-bound starch . . . 164 3e−39 gi|12278507|gb|AAG48994.1| (AY011007) granule-bound starch . . . 164 4e−39 gi|3493117|gb|AAD03016.1| (AF079296) granule-bound starch s . . . 163 5e−39 gi|3493079|gb|AAD02997.1| (AF079277) granule-bound starch s . . . 163 5e−39 gi|12278509|gb|AAG48995.1| (AY011008) granule-bound starch . . . 163 6e−39 gi|3493089|gb|AAD03002.1| (AF079282) granule-bound starch s . . . 163 6e−39 gi|3493065|gb|AAD02990.1| (AF079270) granule-bound starch s . . . 163 6e−39 gi|3493059|gb|AAD02987.1| (AF079267) granule-bound starch s . . . 163 7e−39 gi|3493093|gb|AAD03004.1| (AF079284) granule-bound starch s . . . 162 9e−39 gi|12278497|gb|AAG48989.1| (AY011002) granule-bound starch . . . 162 9e−39 gi|3493113|gb|AAD03014.1| (AF079294) granule-bound starch s . . . 162 9e−39 gi|12278505|gb|AAG48993.1| (AY011006) granule-bound starch . . . 162 9e−39 gi|3493101|gb|AAD03008.1| (AF079288) granule-bound starch s . . . 162 1e−38 gi|12278487|gb|AAG48984.1| (AY010997) granule-bound starch . . . 162 1e−38 gi|3493061|gb|AAD02988.1| (AF079268) granule-bound starch s . . . 162 1e−38 gi|3493049|gb|AAD02982.1| (AF079262) granule-bound starch s . . . 162 1e−38 gi|3493019|gb|AAD02967.1| (AF079247) granule-bound starch s . . . 162 1e−38 gi|12278514|gb|AAG48997.1| (AY011011) granule-bound starch . . . 162 1e−38 gi|12278473|gb|AAG48977.1| (AY010990) granule-bound starch . . . 162 2e−38 gi|3493121|gb|AAD03018.1| (AF079298) granule-bound starch s . . . 162 2e−38 gi|12278481|gb|AAG48981.1| (AY010994) granule-bound starch . . . 162 2e−38 gi|3493025|gb|AAD02970.1| (AF079250) granule-bound starch s . . . 161 2e−38 gi|3493091|gb|AAD03003.1| (AF079283) granule-bound starch s . . . 161 2e−38 gi|3493031|gb|AAD02973.1| (AF079253) granule-bound starch s . . . 161 2e−38 gi|12278471|gb|AAG48976.1| (AY010989) granule-bound starch . . . 161 2e−38 gi|12278463|gb|AAG48972.1| (AY010985) granule-bound starch . . . 161 2e−38 gi|3493067|gb|AAD02991.1| (AF079271) granule-bound starch s . . . 161 2e−38 gi|3493051|gb|AAD02983.1| (AF079263) granule-bound starch s . . . 161 2e−38 gi|13774480|gb|AAK38879.1| (AF353517) granule-bound starch . . . 161 3e−38 gi|12278453|gb|AAG48967.1| (AY010980) granule-bound starch . . . 161 3e−38 gi|12278449|gb|AAG48965.1| (AY010978) granule-bound starch . . . 161 3e−38 gi|12278451|gb|AAG48966.1| (AY010979) granule-bound starch . . . 160 3e−38 gi|13774484|gb|AAK38881.1| (AF353519) granule-bound starch . . . 160 3e−38 gi|12278427|gb|AAG48954.1| (AY010967) granule-bound starch . . . 160 3e−38 gi|13774486|gb|AAK38882.1| (AF353520) granule-bound starch . . . 160 3e−38 gi|12278491|gb|AAG48986.1| (AY010999) granule-bound starch . . . 160 3e−38 gi|13774482|gb|AAK38880.1| (AF353518) granule-bound starch . . . 160 4e−38 gi|13377473|gb|AAK20725.1| (AF318769) granule-bound starch . . . 160 4e−38 gi|3493011|gb|AAD02963.1| (AF079243) granule-bound starch s . . . 160 4e−38 gi|3493073|gb|AAD02994.1| (AF079274) granule-bound starch s . . . 160 4e−38 gi|12278479|gb|AAG48980.1| (AY010993) granule-bound starch . . . 160 5e−38 gi|3493057|gb|AAD02986.1| (AF079266) granule-bound starch s . . . 160 6e−38 gi|3493087|gb|AAD03001.1| (AF079281) granule-bound starch s . . . 160 6e−38 gi|3493023|gb|AAD02969.1| (AF079249) granule-bound starch s . . . 160 6e−38 gi|3493041|gb|AAD02978.1| (AF079258) granule-bound starch s . . . 160 6e−38 gi|3493109|gb|AAD03012.1| (AF079292) granule-bound starch s . . . 160 6e−38 gi|3493081|gb|AAD02998.1| (AF079278) granule-bound starch s . . . 160 6e−38 gi|3493021|gb|AAD02968.1| (AF079248) granule-bound starch s . . . 160 6e−38 gi|12278457|gb|AAG48969.1| (AY010982) granule-bound starch . . . 159 6e−38 gi|3493055|gb|AAD02985.1| (AF079265) granule-bound starch s . . . 159 7e−38 gi|12278477|gb|AAG48979.1| (AY010992) granule-bound starch . . . 159 7e−38 gi|12278499|gb|AAG48990.1| (AY011003) granule-bound starch . . . 159 7e−38 gi|12278489|gb|AAG48985.1| (AY010998) granule-bound starch . . . 159 7e−38 gi|12278511|gb|AAG48996.1| (AY011009) granule-bound starch . . . 159 8e−38 gi|13774488|gb|AAK38883.1| (AF353521) granule-bound starch . . . 159 8e−38 gi|12278485|gb|AAG48983.1| (AY010996) granule-bound starch . . . 159 8e−38 gi|3493095|gb|AAD03005.1| (AF079285) granule-bound starch s . . . 159 8e−38 gi|12278429|gb|AAG48955.1| (AY010968) granule-bound starch . . . 159 8e−38 gi|3493077|gb|AAD02996.1| (AF079276) granule-bound starch s . . . 159 8e−38 gi|3493009|gb|AAD02962.1| (AF079242) granule-bound starch s . . . 159 8e−38 gi|3493027|gb|AAD02971.1| (AF079251) granule-bound starch s . . . 159 1e−37 gi|12278413|gb|AAG48947.1| (AY010960) granule-bound starch . . . 159 1e−37 gi|12278443|gb|AAG48962.1| (AY010975) granule-bound starch . . . 159 1e−37 gi|3493097|gb|AAD03006.1| (AF079286) granule-bound starch s . . . 159 1e−37 gi|3493013|gb|AAD02964.1| (AF079244) granule-bound starch s . . . 159 1e−37 gi|3493015|gb|AAD02965.1| (AF079245) granule-bound starch s . . . 159 1e−37 gi|3493099|gb|AAD03007.1| (AF079287) granule-bound starch s . . . 159 1e−37 gi|3493083|gb|AAD02999.1| (AF079279) granule-bound starch s . . . 159 1e−37 gi|13377475|gb|AAK20726.1| (AF318770) granule-bound starch . . . 158 1e−37 gi|3493115|gb|AAD03015.1| (AF079295) granule-bound starch s . . . 158 2e−37 gi|3493017|gb|AAD02966.1| (AF079246) granule-bound starch s . . . 158 2e−37 gi|12278423|gb|AAG48952.1| (AY010965) granule-bound starch . . . 158 2e−37 gi|12278425|gb|AAG48953.1| (AY010966) granule-bound starch . . . 158 2e−37 gi|12278411|gb|AAG48946.1| (AY010959) granule-bound starch . . . 158 2e−37 gi|12278435|gb|AAG48958.1| (AY010971) granule-bound starch . . . 158 2e−37 gi|3493035|gb|AAD02975.1| (AF079255) granule-bound starch s . . . 158 2e−37 gi|12278495|gb|AAG48988.1| (AY011001) granule-bound starch . . . 158 2e−37 gi|12278501|gb|AAG48991.1| (AY011004) granule-bound starch . . . 158 2e−37 gi|12278419|gb|AAG48950.1| (AY010963) granule-bound starch . . . 158 2e−37 gi|12278421|gb|AAG48951.1| (AY010964) granule-bound starch . . . 158 2e−37 gi|3493037|gb|AAD02976.1| (AF079256) granule-bound starch s . . . 158 2e−37 gi|3493071|gb|AAD02993.1| (AF079273) granule-bound starch s . . . 157 2e−37 gi|12278469|gb|AAG48975.1| (AY010988) granule-bound starch . . . 157 3e−37 gi|3493003|gb|AAD02959.1| (AF079239) granule-bound starch s . . . 157 3e−37 gi|3493001|gb|AAD02958.1| (AF079238) granule-bound starch s . . . 157 3e−37 gi|13194734|gb|AAK15529.1| (AF331953) granule-bound starch . . . 157 3e−37 gi|3493075|gb|AAD02995.1| (AF079275) granule-bound starch s . . . 157 3e−37

[0405] Du-1 Accession: AF023159       NID: g3057119   Mol. wt. (calc) = 188101    Residues = 1674 Seq. ID. No. 883 1 M E M V L R S Q S P L C L R S G P V L I F R P T V A G G G G 31 G T Q S L L R T T R F A R R R V I R C V V A S P G C P N R K 61 S R T A S P N V K V A A Y S N Y A P R L L V E S S S K K S E 91 H H D S S R H R E E T I D T Y N G L S G S D A A E L T S N R 121 D V E I E V D L Q H I S E E E L P G K V S I N A S L G E M E 151 T V D E A E V E E D K F E V D T S G I V L R N V A V R E V D 181 P K D E H N A K D V F V V D S S G T A P D N A A V E E V V D 211 E A E V E E D M V D V D I L G L D L N N A T I E E I D L M E 241 E A L L E N F D V D S P G N A S S G R T Y G G V D E L G E L 271 P S T S V D C I A I N G K R R S L K P K P L P I V R F Q E Q 301 E Q I V L S I V D E E G L I A S S C E E G Q P V V D Y D K Q 331 E E N S T A F D E Q K Q L T D D F P E E G I S I V H F P E P 361 N N D I V G S S K F L E Q K Q E L D G S Y K Q D R S T T G L 391 H E Q D Q S V V S S H G Q D K S I V G V P Q Q I Q Y N D Q S 421 I A G S H R Q D Q S I A G A P E Q I Q S V A G Y I K P N Q S 451 I V G S C K Q H E L I I P E P K K I E S I I S Y N E I D Q S 481 I V G S H K Q D K S V V S V P E Q I Q S I V S H S K P N Q S 511 T V D S Y R Q A E S I I G V P E K V Q S I T S Y D K L D Q S 541 I V G S L K Q D E P I I S V P E K I Q S I V H Y T K P N Q S 571 I V G L P K Q Q Q S I V H I V E P K Q S I D G F P K Q D L S 601 I V G I S N E F Q T K Q L A T V G T H D G L L M K G V E A K 631 E T S Q K T E G D T L Q A T F N V D N L S Q K Q E G L T K E 661 A D E I T I I E K I N D E D L V M I E E Q K S I A M N E E Q 691 T I V T E E D I P M A K V E I G I D K A K F L H L L S E E E 721 S S W D E N E V G I I E A D E Q Y E V D E T S M S T E Q D I 751 Q E S P N D D L D P Q A L W S M L Q E L A E K N Y S L G N K 781 L F T Y P D V L K A D S T I D L Y F N R D L S A V A N E P D 811 V L I K G A F N G W K W R F F T E K L H K S E L A G D W W C 841 C K L Y I P K Q A Y R M D F V F F N G H T V Y E N N N N N D 871 F V I Q I E S T M D E N L F E D F L A E E K Q R E L E N L A 901 N E E A E R R R Q T D E Q R R M E E E R A A D K A D R V Q A 931 K V E V E T K K N K L C N V L G L A R A P V D N L W Y I E P 961 I T T G Q E A T V R L Y Y N I N S R P L V H S T E I W M H G 991 G Y N N W I D G L S F A E R L V H H H D K D C D W W F A D V 1021 V V P E R T Y V L D W V F A D G P P G S A R N Y D N N G G H 1051 D F H A T L P N N M T E E E Y W M E E E Q R I Y T R L Q Q E 1081 R R E R E E A I K R K A E R N A K M K A E M K E K T M R M F 1111 L V S Q K H I V Y T E P L E I H A G T T I D V L Y N P S N T 1141 V L T G K P E V W F R C S F N R W M Y P G G V L P P Q K M V 1171 Q A E N G S H L K A T V Y V P R D A Y M M D F V F S E S E E 1201 G G I Y D N R N G L D Y H I P V F G S I A K E P P M H I V H 1231 I A V E M A P I A K V G G L G D V V T S L S R A V Q D L G H 1261 N V E V I L P K Y G C L N L S N V K N L Q I H Q S F S W G G 1291 S E I N V W R G L V E G L C V Y F L E P Q N G M F G V G Y V 1321 Y G R D D D R R F G F F C R S A L E F L L Q S G S S P N I I 1351 H C H D W S S A P V A W L H K E N Y A K S S L A N A R V V F 1381 T I H N L E F G A H H I G K A M R Y C D K A T T V S N T Y S 1411 K E V S G H G A I V P H L G K F Y G I L N G I D P D I W D P 1441 Y N D N F I P V H Y T C E N V V E G K R A A K R A L Q Q K F 1471 G L Q Q I D V P V V G I V T R L T A Q K G I H L I K H A I H 1501 R T L E R N G Q V V L L G S A P D S R I Q A D F V N L A N T 1531 L H G V N H G Q V R L S L T Y D E P L S H L I Y A G S D F I 1561 L V P S I F E P C G L T Q L V A M R Y G T I P I V H K T G G 1591 L F D T V F D V D N D K E R A R D R G L E P N G F S F D G A 1621 D S N G V D Y A L N R A I S A W F D A R S W F H S L C K R V 1651 M E Q D W S W N R P A L D Y I E L Y R S A S K L

[0406] TABLE XXXI Maize soluble starch synthase IIb (SSIIb) Alignments with other similar proteins-Transit Peptide SEQ Accession a.a a.a. Id.No. Number # (start)                  Sequence                  ending # 884 MAIZE SSIIb 1 GGIYDNRNGLDYHIPVFGSIAKEP----- P-------MHIVHIAVEMAPIAKVGGLGD 46 885  7489826 1201 GGIYDNRNGLDYHIPVFGSIAKEP---- -P-------MHIVHIAVEMAPIAKVGGLGD 1246 886  9502145 1139 GIYDNRNGMDYHIPVSDSIETEN-------Y-------MRIIHIAVEMAPVAKVGGLGD 1183 887  9502143 1156 GIYDNRNGMDYHIPVSDSIETEN-------Y-------MRIIHIAVEMAPVAKVGGLGD 1200 888 17646328 743 GGIYDNRNGMDYHSPVTDSVAKEP------P-------MHIVHIAVEMAPIAKVGGLGD 788 889  4582789 672 GGVFDNKFGMDYHIPVFGGIVKEP------P-------MHIVHIAVEMAPIAKVGGLGD 717 890  7489274 755 GGIFDNKSGMDYHIPVFGGVAKEP------P-------MHIVHIAVEMAPIAKVGGLGD 800 891  2833389 755 GGIFDNKSGMDYHIPVFGGVAKEP------P-------MHIVHIAVEMAPIAKVGGLGD 800 892 15221083 552 GGIFDNKNGLDYHLPVVGGISKEP-------P-------LHIVHIAVEMAPIAKVGGLGD 597 893  4582783 370                   SSATSP-------G-------LYVIHIAAEMAPVAKVGGLGD 397 894 15717885 421                                 -------LHIAHIAAEMAPVAKVGGLAD 441 895 15236819 545                                 -------LYVVHIAAEMAPVAKVGGLGD 565 896 18461221 348                                                    VLQVGGLAD 356 897  8901183 129              MPLQGGAAEAPPVERDGNP-------MHIIHITAEMAPIAKVGGLGD 168 898 17227527 1                                 -------MYIVQIASECAPVIKAGGLGD 21 899 16329217 1                                 -------MYIVQIASECAPVIKAGGLGD 21 900  2811062 1                                 -------MKVLFAVSECAPFAKSGGLAD 21 901 18309046 15                                                EANPFIKTGGLGD 27 902 15903076 1                                 -------MKILFVAAEGAPFSKTGGLGD 21 903 17229371 1                                 -------MRILFVAAEAAPIAKVGGMGD 21 904 15900991 1                                 -------MKILFVAAEGAPFSKTGGLGD 21 905 16124067 1                                 -------MRVLHVCSELFPLLKTGGLAD 21 906 16080147 1                                 -------MKILFAVSECTPFVKSGGLAD 21 907 16273270 1                                 -------MKILHVCSELYPLLKTGGLAD 21 908 15602409 1                                 -------MKVLHACSELYPLLKTGGLAD 21 909 15672681 2                      KER-------K-------MKVLFASSECAPFFKTGGLGD 26 910 17938870 22                                 -------MRILAVTAEMFPFVKTGGLAD 42 911 16119514 1                                 -------MRILAVTAEMFPFVKTGGLAD 21 912 15613648 1                                 -------MNVLHVASECNPFFKTGGLAD 21 913 16331219 1                                 -------MKILFVAAEVSPLAKVGGMGD 21 914 17366711 1                                 -------MKVLFASSECAPFFKTGGLGD 21 915 15805621 28                         -------P-------MRVLHLASEVFPFSRSGGLGD 49 916 15620537 1                                 -------MRILFVAAECAPFAKVGGMGD 21 917 15641730 12                                                EVQGLVKSGGLAD 24 918  7489711 199                  GPLAGPN-------V-------MNVVVVASECAPFCKTGGLGD 227 919 15605532 1                                 -------MKIIHTAIEFAPVIKAGGLGD 21 920 15803938 1                                 -------MQVLHVCSEMFPLLKTGGLAD 21 921 17367076 1                                 -------MRVLHLASEVFPFSRSGGLGD 21 922 16766821 1                                 -------MQVLHVCSEMFPLLKTGGLAD 21 923 16762766 1                                 -------MQVLHVCSEMFPLLKTGGLAD 21 924 15834801 1                                 -------MKITHTAIEFAPVIKAGGLGD 21 925 15966599 1                                 -------MNILSVASEVYPLVKTGGLAD 21 926 15618857 1                                 -------MRIVQVAVEFTPIVKVGGLGD 21 927 17366350 2                                 -------IRVLHLAPEAYPLAKVGGLAD 22 928 15384987 138                  GPLAGPN-------V-------MNVIVVASECSPFCKTGGLGD 166 929  2129898 245                 FESGGEKP-------PPLAGTNVMNIILVSAECAPWSKTGGLGD 281 930  2833384 245                 FESGGEKP-------PPLAGTNVMNIILVSAECAPWSKTGGLGD 281 931 15028467 195                  GPLAGPN-------V-------MNVIVVASECSPFCKTGGLGD 223 932 15643657 1                                 -------MKVVFVSYEVFPFAKVGGLAD 21

[0407] TABLE XXXII Maize soluble starch synthase III (Du I) “GLASS” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                     Sequence                     end # 933 MaizeDuI 47 VVTSLSRAVQDLGH--NVEVIL--PKY----GCL------N--LSNV-------KNL--- 80 934  7489826 1247 VVTSLSRAVQDLGH--NVEVIL--PKY----GCL------N--LSNV-------KNL--- 1280 935  9502145 1184 VVTSLSRAVQDLGH--TVEVIL--PKY----DCL------N--QSSV-------KDL--- 1217 936  9502143 1201 VVTSLSRAIQDLGH--TVEVIL--PKY----DCL------N--QSSV-------KDL--- 1234 937 17646328 789 VVTSLSRAVQDLGH--NVEVIL--PKY----DCL------N--LSNV-------KDL--- 822 938  4582789 718 VVTSLSRAVQDLNH--NVDIIL--PKY----DCL------N--LSNV-------KDL--- 751 939  7489274 801 VVTSLSRAVQDLNH--NVDIIL--PKY----DCL------K--MNNV-------KDF--- 834 940  2833389 801 VVTSLSRAVQDLNH--NVDIIL--PKY----DCL------K--MNNV-------KDF--- 834 941 15221083 598 VVTSLSRAVQELNH--NVDIVF--PKY----DCI------K--HNFV-------KDL--- 631 942  4582783 398 VISGLSKALQKKGH--LVEIIL--PKY----DCM------Q--YDRI-------GDL--- 431 943 15717885 442 VISGLGKALQKKGH--LVEIIL--PKY----DCM------Q--VDQV-------SNL--- 475 944 15236819 566 VVAGLGKALQRKGH--LVEIIL--PKY----DCM------Q--YDRV-------RDL--- 599 945 18461221 357 VVAGLGKALQTKGH--LVEIVL--PKY----DCM------Q--LDQI-------TNL--- 390 946  8901183 169 VVTGLAKAALARGH--FVTVML--PFY----ECL------P--KDQI-------EGLKHE 205 947 17227527 22 VVYGLSRELEIRGN--CVELIL--PKY----DCM------R--YDHV-------WGL--- 55 948 16329217 22 VIYGLSRELELRGH--CVELIL--PMY----DCM------R--YDHIWGLHDAYRNL--- 62 949  2811062 22 VAGALPKELRRLGI--DARVML--PKY----ETIAPEWKKK--MKKV-------AEL--- 61 950 18309046 28 VMGALPKELKRKGI--DARVIL--PKY----SAI------K--GELL-------DKL--- 61 951 15903076 22 VIGALPKSLVKAGH--EVAVIL--PYY----DMVEAEFGNQ--IEDV-------LEF--- 61 952 17229371 22 VVGALPKVLRKMGH--DVRIFL--PYY----GFL------P-------------DKM--- 51 953 15900991 22 VIGALPKSLVKAGH--EVAVIL--PYY----DMVEAKFGNQ--IEDV-------LHF--- 61 954 16124067 22 VIGALPAAQLAEGA--DVRIIL--PAF----PDL------R--RGIP-------ETV--- 55 955 16080147 22 VAGALPKALARLGN--EVAVML--PKY----SQI------P--EPWK-------KEN--- 55 956 16273270 22 VLGALPQAQNQIGL--DARFLL--PAY----PAI------T---TGI-------PNT--- 54 957 15602409 22 VMGALPFAQKEIGI--DARIVL--PAY----PAI------K---AGI-------PET--- 54 958 15672681 27 VAGALPKELAKKSEIDSVAVIL--PYF----KNE------M--KEEY-------RSL--- 62 959 17938870 43 ATSALPQALERKGA--DVRTLL--PLY----RGL------TPLVRGR-------KPV--- 78 960 16119514 22 ATSALPQALERKGA--DVRTLL--PLY----RGL------TPLVRGR-------KPV--- 57 961 15613648 22 VLGSLPKALIKQGI--NVSVIL--PKY----GHL------S--DEWQ-------NQL--- 55 962 16331219 22 VVGSLPKVLHQLGH--DVRVFM--PYY----GFI------G-------------DKI--- 51 963 17366711 22 VAGALPKELAKKSEIDSVAVIL--PYF----KNE------M--KEEY-------RSL--- 57 964 15805621 50 VLGALPAVQARLGE--DAEVTVLSPWY----ASL-----------QG-------EPQ--- 82 965 15620537 22 VVGSLPKVLKASAH--DVGIFM--RYY----GFL------------T-------SKL--- 51 966 15641730 25 VAKALPQALKALHQ--QVAIAL--PAY----RSV------P--GKED-------AEL--- 58 967  7489711 228 VVGALPKALARRGH--RVMVVI--PRY----G--------E--YAEA-------RDL--- 259 968 15605532 22 ALYGLAKALA-ANH--TTEVVI--PLY----PKLF-----T--LPKE-------QDL--- 55 969 15803938 22 VIGALPAAQIADGV--DARVLL--PAF----PDI------R---RGV-------TDA--- 54 970 17367076 22 VLGALPAVQARLGE--DAEVTVLSPWY----ASL-----------QG-------EPQ--- 54 971 16766821 22 VIGALPAAQIADGV--DVRVLL--PGF----PDI------R--RGIP-------DAH--- 55 972 16762766 22 VIGALPAAQIADGV--DVRVLL--PGF----PDI------R--RGIP-------DAH--- 55 973 15834801 22 ALYGLAKALA-VNH--TTEVVI--PLYPKLFTSL------H--EQDL-------FAT--- 58 974 15966599 22 VVGALPSALLPHGV--RTRTLV--PGY----PSV------L--KKLK-------KKK--- 55 975 15618857 22 AVASLSKELAK-QN--DVEVLL--PHY----PLI------S--KFSS-------SQV--- 54 976 17366350 23 VVGALPKALRPLGV--EAHVLL--PWH----GGL------E--ARRV-------GEV--- 56 977 15384987 167 VVGALPKALARRGH--RVMVVI--PRY----G--------E--YAEA-------KDL--- 198 978  2129898 282 VAGSLPKALARRGH--RVMIVA--PHY----G--------N--YAEA-------HDI--- 313 979  2833384 282 VAGSLPKALARRGH--RVMIVA--PHY----G--------N--YAEA-------HDI--- 313 980 15028467 224 VVGALPKALARRGH--RVMVVI--PRY----G--------E--YAEA-------KDL--- 255 981 15643657 22 VAGTLPKYLKKHGV--DVTIVM--PKH----RIV------E---KNA-------EKFGYE 57 933 maizeDu1 81 ---Q-----I-H----Q----SF-----S-----W---G----G----S------EI--N 94 934  7489826 1281 ---Q-----I-H----Q----SF-----S-----W---G----G----S------EI--N 1294 935  9502145 1218 ---H-----L-Y----Q----SF-----S-----W---G----G----T------EI--K 1231 936  9502143 1235 ---H-----L-Y----Q----SF-----S-----W---G----G----T------EI--K 1248 937 17646328 823 ---H-----Y-R----Q----SF-----T-----W---G----N----T------EI--K 836 938  4582789 752 ---Q-----F-H----K----SY-----F-----W---S----G----T------EI--K 765 939  7489274 835 ---R-----F-H----K----NY-----F-----W---G----G----T------EI--K 848 940  2833389 835 ---H-----F-H----K----NY-----F-----W---G----G----T------EI--K 848 941 15221083 632 ---Q-----F-N----R----SY-----H-----W---G----G----T------EI--K 645 942  4582783 432 ---RALDVVI-E----S----YF-----D-----G---Q----L----F------KN--K 450 943 15717885 476 ---K-----V-LDVLVQ----SY-----F-----E---G----N----M------FN--N 493 944 15236819 600 ---RALDTVV-E----S----YF-----D-----G---K----L----Y------KM--K 618 945 18461221 391 ---KVLDVVI-Q----S----YF-----D-----G---N----L----F------SN--N 409 946  8901183 206 CDIE-----V-P----K----GY-----H-----W---D----G----EIRVGPLKT--S 228 947 17227527 56 -----------H----E----AYLNLWVP-----W---F----G----A------AI--H 72 948 16329217 63 ---E-----V------------------P-----W---Y----G----S------SIFCD 74 949  2811062 62 ---I-----V-----------PV-----G-----W---R----R----Q------YC--G 73 950 18309046 62 ---S-----F-K----K----WFMVPV-G-----W---R----N----Q------YC--G 79 952 15903076 62 ---E-----V-----------SV-----G-----W---R----R----Q------YC--G 73 952 17229371 52 ---E-----I-P----K----DP-----I-----W---K----GYAMFQ------DF--T 69 953 15900991 62 ---E-----V-----------SV-----G-----W---R----R----Q------YC--G 73 954 16124067 56 ---L-----V-R----E----ID-----T-----F---A----G-----------RV--A 68 955 16080147 56 ---K-----K-Q----AECTVAV-----G-----W---R----Q----Q------YC--G 73 956 16273270 55 ---Q-----V-V----A----EF-----D-----N---F----A----G------HV--V 68 957 15602409 55 ---T-----V-V----S----EF-----D-----N---F----A----G------HI--V 68 958 15672681 63 ---L-----K-D----E----FY-----DFVDVGW---R----H----E------YV--G 81 959 17938870 79 ---L-----V-A----N----IL-----E-------------------Q------PV--S 89 960 16119514 58 ---L-----V-A----N----IL-----E-------------------Q------PV--S 68 961 15613648 56 ---T-----L-K----K----SF-----T-----V---S----V----T------WR--N 69 962 16331219 52 ---D-----V-P----K----EP-----V-----W---K----G---------------- 61 963 17366711 58 ---L-----K-D----E----FY-----DFVDVGW---R----H----E------YV--G 76 964 15805621 83 ---E-----L-W----R----GE-----A-----W---G----E---------------Q 93 965 15620537 52 ---D-----IPA----E----PI-----W-----W---G----Y----A------MF--N 66 966 15641730 59 ---V-----L-E----T----EL-----TH----W---P----H----T------QY--R 73 967 74897112 60 ---G-----V-R----R----RY-----K-----V---A----GQD--S------EV--T 275 968 15605532 56 ---C-----S-I----Q----KL-----S-----YFFAG----E----Q------EA--T 72 969 15803938 55 ---Q-----V-V----S----RR-----D-----T---F----A----G------HI--T 68 970 17367076 55 ---E-----L-W----R----GE-----A-----W---G----E---------------Q 65 971 16766821 56 ---V-----V-S----R----RD-----T-----F---A----G-----------KI--S 68 972 16762766 56 ---V-----V-S----R----RD-----T-----F---A----G-----------KI--S 68 973 15834801 59 ---Q-----K-I----P----YF-----F-----A---G----E----Q------EA--T 72 974 15966599 56 ---p-----V-G----R----FD-----N-----L---F----G----H------PA--T 69 975 15618857 55 ---L-----S-E----R----SF-----Y-----YEFLG----K----Q------QA--S 71 976 17366350 57 ---------------------AF-----A-----F---F----G----R------EE--R 66 977 15384987 199 ---G-----V-R----K----RY-----R-----V---A----GQD--S------EV--S 214 978  2129898 314 ---G-----V-R----K----RY-----K-----V---A----G----QDM----EV--T 329 979  2833384 314 ---G-----V-R----K----RY-----K-----V---A----G----QDM----EV--T 329 980 15028467 256 ---G-----V-R----K----RY-----R-----V---A----GQD--S------EV--S 271 981 15643657 58 IK-K-----V-A----E----SL-----S-----V---SHVKTD----Q------KF--D 77 933 Maize Du1 95 ---VWRG-LV----EG--LCV--Y--F--LE-----P-----------Q---NG---M-- 114 934  7489826 1295 ---VWRG-LV----EG--LCV--Y--F--LE-----P-----------Q---NG---M-- 1314 935  9502145 1232 ---VWVG-RV----ED--LTV--Y--F--LE-----P-----------Q---NG---M-- 1251 936  9502143 1249 ---VWVG-RV----ED--LTV--Y--F--LE-----P-----------Q---NG---M-- 1268 937 17646328 837 ---VWFG-KV----ED--VPV--Y--F--LE-----P-----------Q---NG---M-- 856 938  4582789 766 ---VWHG-KV----EG--LSV--Y--F--LE-----P-----------Q---NG---LF- 786 939  7489274 849 ---VWFG-KV----EG--LSV--Y--F--LE-----P-----------Q---NG---LF- 869 940  2833389 849 ---VWFG-KV----EG--LSV--Y--F--LE-----P-----------Q---NG---LF- 869 941 15221083 646 ---VWHG-KV----EG--LSV--Y--F--LD-----P-----------Q---NG---LF- 666 942  4582783 451 ---IWVG-TV----EG--LPV--Y--F--IE-----P-----------H---HPGKFF-- 473 943 15717885 494 K--IWTG-TV----EG--LPV--Y--F--IE-----P-----------Q---HPAMFF-- 517 944 15236819 619 ---IWIG-TV----EG--LPV--H--F--IE-----P-----------Q---HPSKFF-- 641 945 18461221 410 ---VWTG-TV----EG--LPV--Y--F--IE-----P-----------Q---HPSKFF-- 432 946  8901183 229 ---VFWG-RV----QG--CPV--Y--L--IK-----P-----------A---DD---TNC 250 947 17227527 73 CT-VYCG-WV----HG--RVC--F--F--IE-----P-----------HSEDNF---F-- 97 948 16329217 75 ---VFCG-WV----HG--RLC--F--F--IQ-----P-----------KSSDNF---F-- 97 949  2811062 74 ---VEEL-RH----DG--VIY--Y--F--ID-----N-----------E---YY---F-- 93 950 18309046 80 ---VYQC-EY----DE--VIY--Y--L--LD-----S-----------E---FY---F-- 99 951 15903076 74 ---IKKT-VL----NG--VTF--Y--F--ID-----N-----------Q---YY---F-- 93 952 17229371 70 ---VHEA-VL----PG--TDVP-L--Y--LF-----G-----------H---PA---F-- 90 953 15900991 74 ---IKKT-VL----NG--VTF--Y--F--ID-----N-----------Q---YY---F-- 93 954 16124067 69 ---LRYG-HY----RG--IGI--Y--L--ID-----APALYDRAGSPYH---DA---S-- 99 955 16080147 74 ---IEHM-AE----ND--VNY--Y--F--ID-----N-----------E---YY---F-- 93 956 16273270 69 ---LRYG-EY----NG--VGI--Y--L--ID-----A-----------P---HL---Y-- 88 957 15602409 69 ---LRYG-EY----KG--LGV--Y--L--IDA----P-----------H---LY---Q-- 89 958 15672681 82 ---VKSL-EK----EG--VKY--Y--F--LD-----N-----------E---HY---F-- 101 959 17938870 90 ---VYYV-VS----DG--HKL--L--L--LE-----A-----------A---SL---F-- 109 960 16119514 69 ---VYYV-VS----DG--HKL--L--L--LE-----A-----------A---SL---F-- 88 961 15613648 70 ---QYCG-LEQFVDQG--VTY--Y--F--ID-----N-----------E---YY---F-- 93 962 16331219 62 -----EA-MF----QQ--FAV--YQSY--L------P-----------D---TK---I-- 80 963 17366711 77 ---VKSL-EK----EG--VKY--Y--F--LD-----N-----------E---HY---F-- 96 964 15805621 94 ---AWLG-EL----RQ--DGV--R--Y--LF-----L-----------G---LN---E-- 113 965 15620537 67 HFAVYET-QL----PG--SDVP-L--Y--LM-----G-----------H---PA---9-- 90 966 15641730 74 ---VLKR-DL----DG--VPI--Y--L--IDCPAYFD-----------R---PA---L-- 98 967  7489711 276 ---YFHS-YI----DG--VDF--V--F--VE-----APPF--------R---HR---H-- 298 968 15605532 73 ---AFSY-FY----EG--IKVTLF--K--LD-----T-----------Q---PE---L-- 94 969 15803938 69 ---LLFG-HY----NG--VGI--Y--L--ID-----A-----------P---H------- 86 970 17367076 66 ---AWLG-EL----RQ--DGV--R--Y--LF-----L-----------G---LN---E-- 85 971 16766821 69 ---LLFG-HY----NG--VGI--Y--L--IDA----P-----------H---LY---E-- 89 972 16762766 69 ---LLWG-HY----NG--VGI--Y--L--IDA----P-----------H---LY---S-- 89 973 15834801 73 ---AFSY-FY----EG--IKV--T--LLKLD-----S-----------Q---PE---L-- 94 974 15966599 70 ---VLAA-EV----NG--VDL--L--V--LD-----Q-----------P---AL---Y-- 89 975 15618857 72 ---AISY-SY----EGLTLTI--I--T--LD-----S-----------Q---IE---L-- 93 976 17366350 67 ---APLGERV----EG--GVR--F--L--LL-----G-----------V---EG---F-- 87 977 15384987 215 ---YFHA-FI----DG--VDF--V--F--LE-----APPF--------R---HR---H-- 237 978  2129898 330 ---YFHT-YI----DG--VDI--V--F--ID-----SPIF--------R---NL---E-- 352 979  2833384 330 ---YFHT-YI----DG--VDI--V--F--ID-----SPIF--------R---NL---E-- 352 980 15028467 272 ---YFHA-FI----DG--VDF--V--F--LE-----APPF--------R---HR---H-- 294 981 15643657 78 ---IYES-VL----PG--SDVKTY--F--VA-----N-----------D---YY---F-- 99 933 maizeDu-1 115 ----XXXXXXXXXXXXXXXXXXCR---------SA--------L--------E---FL-L 141 934  7489826 1315 ----FGVGYVYGRDDDRRFGFFCR---------SA--------L--------E---FL-L 1341 935  9502145 1252 ----FGVGCVYGRNDDRRFGFFCH---------SA--------L--------E---FI-L 1278 936  9502143 1269 ----FGVGCVYGRNDDRRFGFFCH---------SA--------L--------E---FI-L 1295 937 17646328 857 ----FWVGCVYGRNDESRFGFFCH---------SA--------L--------E---FL-R 883 938  4582789 787 ----NVGCVYGRANDAERFGFFCH---------AA--------L--------E---FL-L 813 939  7489274 870 ----SKGCVYGCSNDGERFGFFCR---------AA--------L--------E---FL-L 896 940  2833389 870 ----SKGCVYGCSNDGERFGFFCH---------AA--------L--------E---FL-L 896 941 15221083 667 ----QRGCVYGCADDAGRFGFFCH---------AA--------L--------E---FL-L 693 942  4582783 474 ----WRGDYYGAHDDFRRFSYFSR---------AA--------L--------E---FL-L 500 943 15717885 518 ----SRAQYYGEHDDFKRFSYFSR---------AA--------L--------E---LL-Y 544 944 15236819 642 ----WRGQFYGEQDDFRRFSYFSR---------AA--------L--------E---LL-L 668 945 18461221 433 ----WRAQYYGEHDDFKRYSYFSR---------AA--------L--------E---LL-Y 459 946  8901183 251 NIFRGGRIYGGSYNEMEAYLYFCR---------AC--------L--------E---YL-N 281 947 17227527 98 ----NRGCYYGCDDDDMRFAFFSK---------AA--------L--------E---FL-H 124 948 16329217 98 ----NRGHYYGALDDHMRFAFFSK---------AA--------M--------E---FL-L 124 949  2811062 94 ----KRPQLYGHYDDGERFAYFCR---------AV--------L--------E---VL-P 120 982  7484399 62                       CR---------AC--------L--------E---YLNV 71 950 18309046 100 ----HRNGLYGEGDDGERFAFFDR---------AV--------L--------E---TL-K 126 951 15903076 94 ----FRGHVYGDFDDGERFAFFQL---------AA--------I--------E---AM-E 120 952 17229371 91 ----TPRRIYSGDDEDWRFTLFSN---------GA--------A--------E---FC-W 117 953 15900991 94 ----FRGHVYGDFDDGERFAFFQL---------AA--------I--------E---AM-E 120 954 16124067 100 ----LYAYSDNYLRFALLGWMACE---------LA--------C--------G------L 124 955 16080147 94 ----NRDSLYGHYDDGERFAFFSR---------AV--------L--------E---AA-K 120 956 16273270 89 ----GREGNPYHDAYYNDYGDNYKRFALLGWVGAE--------L--------A---TG-L 124 957 15602409 90 ----REGNPYHDQWYNDYADNYKR---------FALLGWVAAEL--------A---TG-L 124 958 15672681 102 ----GRGQLYGYGDDGERFAFFDL---------AL--------C--------Q---LL-E 128 959 17938870 110 ----DRDGHPYGVKGEPFADNDLR---------FA--------VLSKVAA--E---IA-L 142 960 16119514 89 ----DRDGHPYGVKGEPFADNDLR---------FA--------VLSKVAA--E---IA-L 121 961 15613648 94 ----KRERLYGYLDEAERFTFFNH---------AV--------L--------S---SL-P 120 962 16331219 81 ----PLYLFGHPAFDSRRIYGGDD---------EA--------W--------R---FT-F 107 963 17366711 97 ----GRGQLYGYGDDGERFAFFDL---------AL--------C--------Q---LL-E 123 964 15805621 114 ----FQRPGLYHPDDVERFCAFGR---------AA--------L--------P---AL-D 140 965 15620537 91 ----DPHRIYSGEDEDWRFTFFAN---------GA--------A--------E---FS-W 117 966 15641730 99 ----YAENNQAYADNGERFGFFSA---------AC--------L--------D---VL-P 125 967  7489711 299 ----NNIYGGERLDILKRMILFCK---------AA--------V--------E---VP-W 325 968 15605532 95 ----FENAETIYTSDDAFRFCAFS---------AA--------A--------A---SY-I 121 969 15803938 87 -----LYDRPGSPYHDTNLFAYTD---------NV--------L--------R---FA-L 112 970 17367076 86 ----FQRPGLYHPDDVERFCAFGR---------AA--------L--------P---AL-D 112 971 16766821 90 ----RPGSPYHDTNLYAYTDNVLR---------FA--------LLGWVGCEMA---CG-L 124 972 16762766 90 ----RPGSPYHDTNLYAYIDNVLR---------FA--------LLGWVGCEMA---CG-L 124 973 15834801 95 ----FEEAETIYTNDDAFRFCAFS---------AA--------A--------A---AY-I 121 974 15966599 90 ----ARDGGPYLDSTGRDYPDNFR---------RF--------A--------A---LS-L 116 975 15618857 94 ----FSTTSVYSENNVVRFSAFAA---------AA--------A--------A---Y--L 119 976 17366350 88 ----GRERVYGYPDDAERYLRFAL---------AA--------K--------E---V--- 112 977 15384987 238 ----NDIYGGERFDVLKRMILFCK---------AA--------V--------EVPWFA-P 267 978  2129898 353 ----SNIYGGNRLDILRRMVLFCK---------AA--------V--------E---VP-W 379 979  2833384 353 ----SNIYGGNRLDILRRMVLFCK---------AA--------V--------E---VP-W 379 980 15028467 295 ----NDIYGGERFDVLKRMILFCK---------AA--------V--------EVPWFA-P 324 981 15643657 100 ----SAEDVYAGPDLGEQAIFFCA---------AT--------L--------D---LV-K 126 933 MaizeDu1 142 --------QS-------GS----------S---------PNIIH-CNDWSS--A--PV-A 161 934  7489826 1342 --------QS-------GS----------S---------PNIIH-CHDWSS--A--PV-A 1361 935  9502145 1279 --------QN-------EF----------S---------PHIIH-CHDWSS--A--PV-A 1298 936  9502143 1296 --------QN-------EF----------S---------PHIIH-CHDWSS--A--PV-A 1315 937 17646328 884 --------QN-------GS----------S---------PDIIH-CHDWSS--A--PV-A 903 938  4582789 814 --------QN-------GS----------H---------PDIIH-CHDWSS--A--PV-A 833 939  7489274 897 --------QG-------GF----------S---------PDIIH-CHDWSS--A--PV-A 916 940  2833389 897 --------QG-------GF----------S---------PDIIH-CHDWSS--A--PV-A 916 942 15221083 694 --------QG-------GF----------H---------PDILH-CHDWSS--A--PV-S 713 942  4582783 501 --------QA-------GK----------K---------PDIIH-CHDWQT--A--FI-A 520 943 15717885 545 --------QS-------GK----------K---------VDIIH-CHDWQT--A--FV-A 564 944 15236819 669 --------QS-------GK----------K---------PDIIH-CHDWQT--A--FV-A 688 945 18461221 460 --------QS-------GK----------K---------IDIIH-CHDWQT--A--FV-A 479 946  8901183 282 --------VS-------QQ----------N---------PHVLQ-LHDWHA--A--AA-S 301 947 17227527 125 --------QS-------NK----------R---------PDIIH-CHDWQT--G--LI-P 144 948 16329217 125 --------RS-------NK----------R---------PDIIH-CHDWQT--G--LV-P 144 949  2811062 121 --------EI-------QF----------Q---------PDVIH-CHDWHT--G--MV-P 140 982  7484399 72 --------SQ-------QQ----------N---------PHVLQ-LHDWHA--A--AA-S 91 950 18309046 127 --------EI-------DW----------C---------PDIIH-CNDWQT--G--MI-P 146 951 15903076 121 --------RI-------DF----------I---------PDLLH-VHDYHT--A--MI-P 140 952 17229371 118 --------NY-------W-----------K---------PDIIH-CHDWHT--G--MIPV 137 953 15900991 121 --------RI-------DF----------I---------PDLLH-VHDYHT--A--MI-P 140 954 16124067 125 --------DG-------YW----------R---------PEVVH-AHDWHA--G--LT-C 144 955 16080147 121 --------VV-------NV----------Q---------ADIVH-THDWHT--A--MV-N 140 956 16273270 125 --------DS-------WW----------R---------AEVVH-AHDWHA--GL-CV-A 145 957 15602409 125 --------DS-------WW----------H---------ADVVH-AHDWHAGLA--SA-Y 146 958 15672681 129 --------KL-------DF----------I---------PDVLH-VNDWQT--A--MV-P 148 959 17938870 143 --------GAID-----GW----------Q---------PDVVH-VHDWHA--A--LT-C 164 960 16119514 122 --------GAID-----GW----------Q---------PDVVH-VHDWHA--A--LT-C 143 961 15613648 121 --------FL-------DE----------S---------PDLIH-CHDWQS--G--LI-P 140 962 16331219 108 --------FS-------NG----------AAEFAWNHWKPEIIH-CHDWHT--G--MIPV 137 963 17366711 124 --------KL-------DF----------I---------PDVLH-VNDWQT--A--MV-P 143 964 15805621 141 --------AV-------GV----------T---------PDVLH-GHDWQA--G--LV-V 160 965 15620537 118 --------NY-------W-----------K---------PQVIH-CHDWHT--G--MIPV 137 966 15641730 126 --------KL-------GI----------Q---------PDIIH-ANDWHT--G--LV-P 145 967  7489711 326 --------YAPCGGTVYGD----------G---------NLVFI-ANDWHT--A--LL-P 352 968 15605532 122 --------QK--------E----------G---------ANIVH-LHDWHT--G--LV-A 140 969 15803938 113 LGWVGAEMAS-------GL----------DPFWR-----PDVVH-AHDWHAGLA--PA-Y 146 970 17367076 113 --------AV-------GV----------T---------PDVLH-GHDWQA--G--LV-V 132 971 16766821 125 --------DP-------FW----------R---------PDVVH-AHDWHAGLA--PA-Y 146 972 16762766 125 --------DP-------FW----------R---------PDVVH-AHDWHAGLA--PA-Y 146 973 15834801 122 --------QK--------E----------G---------ADIVH-LHDWHV--G--LV-A 140 974 15966599 117 --------AA-------AEIAGNGIIPNWK---------PDIVH-VHDWQT--ALTPV-- 147 975 15618857 120 --------QE-------AD----------P---------ADIVH-LHDWHV--G--LL-A 139 976 17366350 113 -----------------AR----------G---------YDLVH-AHDWTA--A--LL-A 130 977 15384987 268 --------CG-------GSIYG-------D---------GNLVFIANDWHT--A--LL-P 291 978  2129898 380 --------HVPCGGICYGD----------G---------NLVFI-ANDWHT--A--LL-P 406 979  2833384 380 --------HVPCGGICYGD----------G---------NLVFI-ANDWHT--A--LL-P 406 980 15028467 325 --------CG-------GSIYG-------D---------GNLVFIANDWHT--A--LL-P 348 981 15643657 127 --------HL-------DL----------K---------PDIVH-VNDWQT--A--LI-P 146 933 Maize Du1 162 WLHKENYA-KSS-L-A-N-ARVV---------------FTIHN----------------- 184 934  7489826 1362 WLHKENYA-KSS-L-A-N-ARVV---------------FTIHN----------------- 1384 935  9502145 1299 WLYKEHYS-QSR-M-A-S-TRVV---------------FTIHN----------------- 1321 936  9502143 1316 WLYKEHYS-QSR-M-A-S-TRVV---------------FTIHN----------------- 1338 937 17646328 904 WLFKEQYA-QNG-L-S-N-GRVV---------------FTIHN----------------- 926 938  4582789 834 WLFKEQYT-HYG-L-S-K-ARVV---------------FTIHN----------------- 856 939  7489274 917 WLFKEQYT-HYG-L-S-K-SRIV---------------FTIHN----------------- 939 940  2833389 917 WLFKEQYT-HYG-L-S-K-SRIV---------------FTIHN----------------- 939 941 15221083 714 WLFKDHYT-QYG-L-I-K-TRIV---------------FTIHN----------------- 736 942  4582783 521 PLYWDVYA-FKG-L-N-S-ARIC---------------FTCHN----------------- 543 943 15717885 565 PLYWDVYA-NLG-F-N-S-ARIC---------------FTCHN----------------- 587 944 15236819 689 PLYWDLYA-PKG-L-D-S-ARIC---------------FTCHN----------------- 711 945 18461221 480 PLYWDIYA-TRG-F-S-S-ARIC---------------FTCHN----------------- 502 946  8901183 302 MLYWDVYN-PNG-F-S-R-TRLM---------------LTIHN----------------- 324 947 17227527 145 VMLYEIYK-YHG-M-D-T-QRVC---------------YTIHN----------------- 167 948 16329217 145 VLLYEIYR-FHG-M-D-H-QRVC---------------YTIHN----------------- 167 949  2811062 141 FLLREQYR-HEL-FYV-D-MRTV---------------FTIHN----------------- 164 982  7484399 92 MLYWDVYN-PNG-F-S-R-TRLM---------------LTIHN----------------- 114 950 18309046 147 VLHKLEYS-KDP-FYK-N-IKTV---------------TSIHN----------------- 170 951 15903076 141 FLLKEKYRWIQA-Y-E-D-IETV---------------LTIHN----------------- 164 952 17229371 138 WMNQS----------P-D-ITTV---------------FTIHN----------------- 153 953 15900991 141 FLLKEKYRWIQA-Y-E-D-IETV---------------LTIHN----------------- 164 954 16124067 145 -----AYL-AAR-G-R-P-ARSV---------------FTVHN----------------- 162 955 16080147 141 YLLKEEYR-KHP-FYE-R-MKSV---------------LTIHN----------------- 164 956 16273270 146 YLFNKGKP-----------AKSV---------------FTIHN----------------- 162 957 15602409 147 LFNKGRPA-KS-----------V---------------FTIHN----------------- 162 958 15672681 149 FLLKEKYNWIKA-Y-E-K-IKTV---------------LTIHN----------------- 172 959 17938870 165 V-----YL-ADS-T-P-S-VASV---------------LTLHN----------------- 182 960 16119514 144 V-----YL-ADS-T-P-S-VASV---------------LTLHN----------------- 161 961 15613648 141 AYMKTGSV-ENP-V-P-----TV---------------FTIHNLRYQGAFPPDVFREL-- 175 962 16331219 138 WMHQS----------P-D-IATV---------------FTIHN----------------- 153 963 17366711 144 FLLKEKYNWIKA-Y-E-K-IKTV---------------LTIHN----------------- 167 964 15805621 161 -------A-HAR-L-R-G-LRTA---------------FSVHN----------------- 176 965 15620537 138 WMHQS----------P-D-ISTV---------------FTIHN----------------- 153 966 15641730 146 FLLKTRYR-YDSFF-E-Q-VKSV---------------LTVHNAIFKGIFSYHQLEVIPE 186 967  7489711 353 VYLKAYYR-DNG-L-M-QYARSV---------------LVIHN----------------- 376 968 15605532 141 GLLKQQPC--SQ-L-----QKIV---------------LTLHN----------------- 160 969 15803938 147 LAARGRPA-KS-----------V---------------FTVHN----------------- 162 970 17367076 133 -------A-HAR-L-R-G-LRTA---------------FSVHN----------------- 148 971 16766821 147 LAARGRPA-KS-----------V---------------FTVHN----------------- 162 972 16762766 147 LAARGRPA-KS-----------V---------------FTVHN----------------- 162 973 15834801 141 GLLKQQPC-PQL-------QKIV---------------LTLHN----------------- 160 974 15966599 148 ------YM-RFG-P-APD-LPTV---------------MTIHN----------------- 165 975 15618857 140 GLLKNPL----N-P-V-H-SKIV---------------FTIHN----------------- 159 976 17366350 131 LYAPTVYT-IHN-L-A-H-QGLVDPGLFFSWTGLPWSLFHMEA----------------- 168 977 15384987 292 VYLKAYYR-DNG-L-M-QYTRSV---------------LVIHNIAHQGRGPVDDFAT--- 329 978  2129898 407 VYLKAYYR-DHG-L-M-NYTRSV---------------LVIHN----------------- 430 979  2833384 407 VYLKAYYR-DHG-L-M-NYTRSV---------------LVIHN----------------- 430 980 15028467 349 VCLKAYYR-DNG-L-M-QYTRSV---------------LVIHNIAHQGRGPVDDFAT--- 386 981 15643657 147 VYLKTVYR-DDPYF-S-R-TATV---------------LTIHN----------------- 170 933 maizeDu1 185 --------L-----------------E--------------------------------- 186 934  7489826 1385 --------L-----------------E--------------------------------- 1386 935  9502145 1322 --------L-----------------E--------------------------------- 1323 936  9502143 1339 --------L-----------------E--------------------------------- 1340 937 17646328 927 --------L-----------------E--------------------------------- 928 938  4582789 857 --------L-----------------E--------------------------------- 858 939  7489274 940 --------L-----------------E--------------------------------- 941 940  2833389 940 --------L-----------------E--------------------------------- 941 941 15221083 737 --------L-----------------E--------------------------------- 738 942  4582783 544 --------L-----------------E--------------------------------- 545 943 15717885 588 --------L-----------------E--------------------------------- 589 944 15236819 712 --------L-----------------E--------------------------------- 713 945 18461221 503 --------L-----------------E--------------------------------- 504 946  8901183 325 --------L-----------------D--------------------------------- 326 947 17227527 168 --------F-----------------KHQGIGGVKTLWATGLNREAYYFQDDKLRDDHNP 202 948 16329217 168 --------F-----------------E--------------------------------- 169 949  2811062 165 --------L-----------------E--------------------------------- 166 982  7484399 115 --------L-----------------E--------------------------------- 116 950 18309046 171 --------L-----------------E--------------------------------- 172 951 15903076 165 --------L-----------------E--------------------------------- 166 952 17229371 154 --------L-----------------E--------------------------------- 155 953 15900991 165 --------L-----------------E--------------------------------- 166 954 16124067 163 --------L-----------------AYQGL----------------------------- 168 955 16080147 165 --------L-----------------E--------------------------------- 166 956 16273270 163 --------LAYQG-------------Q--------------------------------- 168 957 15602409 163 --------LAYQG-------------Q--------------------------------- 168 958 15672681 173 --------I-----------------E--------------------------------- 174 959 17938870 183 --------L-----------------A--------------------------------- 184 960 16119514 162 --------L-----------------A--------------------------------- 163 961 15613648 176 --------L-----------------H--------------------------------- 177 962 16331219 154 --------L-----------------A--------------------------------- 155 963 17366711 168 --------I-----------------E--------------------------------- 169 964 15805621 177 --------L-----------------QYQGRWNLHEAAGWTGLPDWTFGPDGVEF----- 206 965 15620537 154 --------L-----------------A--------------------------------- 155 966 15641730 187 LNLSGMEFL-----------------Q--------------------------------- 196 967  7489711 377 --------IAHQGRGPVDDFVNF---D--------------------------------- 392 968 15605532 161 --------F-----------------G--------------------------------- 162 969 15803938 163 --------L-----------------AYQGM----------------------------- 168 970 17367076 149 --------L-----------------QYQGRWNLHEAAGWTGLPDWTFGPDGVEF----- 178 971 16766821 163 --------L-----------------A--------------------------------- 164 972 16762766 163 --------L-----------------A--------------------------------- 164 973 15834801 161 --------FGYRGYTTREVLEASSLNE--------------------------------- 179 974 15966599 166 --------IAFQG-------------Q--------------------------------- 171 975 15618857 160 --------FGYRGYCSTQLLAASQIDD--------------------------------- 178 976 17366350 169 --------L-----------------E--------------------------------- 170 977 15384987 330 --------M-----------------D--------------------------------- 331 978  2129898 431 --------I-----------------AHQGRGPVEDFNTVDLSGNYLDLFKMYDP----- 460 979  2833384 431 --------I-----------------AHQGRGPVEDFNTVDLSCNYLDLFKMYDP----- 460 980 15028467 387 --------M-----------------D--------------------------------- 388 981 15643657 171 --------L-----------------G--------------------------------- 172

[0408] TABLE XXXIII Maize soluble starch synthase III (Du I) “LINKR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                     Sequence                     end # 983 MaizeDuI 187 F-----------------------------GA---------------------------- 189 984  7489826 1387 F-----------------------------GA---------------------------- 1389 985  9502145 1324 F-----------------------------GA---------------------------- 1326 986  9502143 1341 F-----------------------------GA---------------------------- 1343 987 17646328 929 F-----------------------------GA---------------------------- 931 988  4582789 859 F-----------------------------GA---------------------------- 861 989  7489274 942 F-----------------------------GA---------------------------- 944 990  2833389 942 F-----------------------------GA---------------------------- 944 991 15221083 739 F-----------------------------GA---------------------------- 741 992  4582783 546 YQGTAGASELEACGLDSHQLNRPDRMQDN-SA---------------------------- 576 993 15717885 590 YQGTAPARDLAWCGL---------------DV---------------------------- 606 994 15236819 714 YQGTA-------------------------SA---------------------------- 720 995 18461221 505 Y-----------------------------QG---------------------------- 507 996  8901183 327 N-----------------------------TG---------------------------- 329 997 17227527 203 F-----------------------------AL---------------------------- 205 998 16329217 170 HQGIA-------------------------GANIL------------------------- 179 999  2811062 167 F-----------------------------QGLFPRGILEDLLNLDGRYFTVDHLEFYGC 197 1000  7484399 117 N-----------------------------TG---------------------------- 119 1001 18309046 173 FQGNFSADVLPELFGYDYEPVRNGSLEFYGGM---------------------------- 204 1002 15903076 167 F-----------------------------QG---------------------------- 169 1003 17229371 156 YQGPWRWYLDKITWCPWYMQ----------GH---------------------------- 177 1004 15900991 167 F-----------------------------QG---------------------------- 169 1005 16124067 169 F-----------------------------SA---------------------------- 171 1006 16080147 167 F-----------------------------QGIFPPDVT--------------------- 176 1007 16273270 169 F-----------------------------SY---------------------------- 171 1008 15602409 169 F-----------------------------AY---------------------------- 171 1009 15672681 175 F-----------------------------QG---------------------------- 177 1010 17938870 185 FQ----------------------------GQ---------------------------- 188 1011 16119514 164 FQ----------------------------GQ---------------------------- 167 1012 15613648 178 F-----------------------------AP---------------------------- 180 1013 16331219 156 YQGPWRGLLETMTWCPWYMQ----------GD---------------------------- 177 1014 17366711 170 F-----------------------------QG---------------------------- 172 1015 15805621 207 F-----------------------------GD---------------------------- 209 1016 15620537 156 YQGPWRWKLEKITWCPWYMQ----------GD---------------------------- 177 1017 15641730 197 Y-----------------------------GH---------------------------- 199 1018  7489711 393 L-----------------------------PE---------------------------- 395 1019 15605532 163 Y-----------------------------RG---------------------------- 165 1020 15803938 169 F-----------------------------YA---------------------------- 171 1021 17367076 179 F-----------------------------GD---------------------------- 181 1022 16766821 165 Y-----------------------------QG---------------------------- 167 1023 16762766 165 Y-----------------------------QG---------------------------- 167 1024 15834801 180 F-----------------------------YL---------------------------- 182 1025 15966599 172 F-----------------------------GA---------------------------- 174 1026 15618857 179 F-----------------------------HL---------------------------- 181 1027 17366350 171 FY----------------------------GR---------------------------- 174 1028 15384987 332 L-----------------------------PE---------------------------- 334 1029  2129898 461 V-----------------------------GG---------------------------- 463 1030  2833384 461 V-----------------------------GG---------------------------- 463 1031 15028467 389 L-----------------------------PE---------------------------- 391 1032 15643657 173 YQGVFDPKYLSFAGLPDYVYTID-------GL---------------------------- 197 983 maizeDu1 190 -H------------------------H-----------------------------I--- 192 984  7489826 1390 -H------------------------H-----------------------------I--- 1392 985  9502145 1327 -H------------------------Y-----------------------------I--- 1329 986  9502143 1344 -H------------------------Y-----------------------------I--- 1346 987 17646328 932 -H------------------------H-----------------------------I--- 934 988  4582789 862 -N------------------------L-----------------------------I--- 864 989  7489274 945 -D------------------------L-----------------------------I--- 947 990  2833389 945 -D------------------------L-----------------------------I--- 947 991 15221083 742 -N------------------------A-----------------------------I--- 744 992  4582783 577 -H------------------------NRVNS-------------------------V--- 583 993 15717885 607 -E------------------------H-----------------------------L--- 609 994 15236819 721 -S------------------------E-----------------------------L--- 723 995 18461221 508 -T------------------------A-----------------------------P--- 510 996  8901183 330 -ETRQDEFFFTGVPGENFA-------T-----------------------------I--- 349 997 17227527 206 -N------------------------Y-----------------------------M--- 208 998 16329217 180 -H------------------------A-----------------------------T--- 182 999  2811062 198 VS------------------------F-----------------------------M--- 201 1000  7484399 120 -ETRQDEFFFTGVPGENFA-------T-----------------------------I--- 139 1001 18309046 205 -S------------------------F-----------------------------M--- 207 1002 15903076 170 -Q------------------------FSEGMLGDLFGVGFERYADGTLRWNNCLNWM--- 201 1003 17229371 178 -N------------------------T-----------------------------M--- 180 1004 15900991 170 -Q------------------------FSEGMLGDLFGVGFERYADGTLRWNNCLNWM--- 201 1005 16124067 172 -D------------------------H-----------------------------L--- 174 1006 16080147 177 -H------------------------DL----------------------------L--- 180 1007 16273270 172 -H------------------------HLYEIGLPTGMFHVEGLELFGQISY-----L--- 198 1008 15602409 172 -H------------------------HLVEIGLPAGMFHVDGLELHGQISY-----L--- 198 1009 15672681 178 -L------------------------M-----------------------------H--- 180 1010 17938870 189 -Y------------------------P-----------------------------L--- 191 1011 16119514 168 -Y------------------------P-----------------------------L--- 170 1012 15613648 181 -E------------------------HFAGLEMDGAINF-----------------L--- 195 1013 16331219 178 -N------------------------V-----------------------------M--- 180 1014 17366711 173 -L------------------------M-----------------------------H--- 175 1015 15805621 210 -L------------------------N-----------------------------L--- 212 1016 15620537 178 -S------------------------T-----------------------------M--- 180 1017 15641730 200 -D------------------------H-----------------------------V--- 202 1018  7489711 396 -H------------------------Y-----------------------------IDHF 401 1019 15605532 166 -Y------------------------TTREILEASSLNEFYISQYQLFRDPQTCV-L--- 196 1020 15803938 172 -H------------------------H-----------------------------M--- 174 1021 17367076 182 -L------------------------N-----------------------------L--- 184 1022 16766821 168 -M------------------------F-----------------------------Y--- 170 1023 16762766 168 -M------------------------F-----------------------------Y--- 170 1024 15834801 183 -S------------------------HYQLFRDPQTCV------------------L--- 196 1025 15966599 175 -SVFPELALPPDAFSTQFVEYYGDVGF-----------------------------L--- 201 1026 15618857 182 -S------------------------HYQLFRDPQTSV------------------L--- 195 1027 17366350 175 -V------------------------N-----------------------------L--- 177 1028 15384987 335 -H------------------------Y-----------------------------IDHF 340 1029  2129898 464 -E------------------------HFNI--------------------------F--- 469 1030  2833384 464 -E------------------------HFNI--------------------------F--- 469 1031 15028467 392 -H------------------------Y-----------------------------IDF- 397 1032 15643657 198 -E------------------------F-----------------------------Y--- 200 983 maize DuI 193 --------------G-------------------K------------------------- 194 984  7489826 1393 --------------G-------------------K------------------------- 1394 985  9502145 1330 --------------G-------------------K------------------------- 1331 986  9502143 1347 --------------G-------------------K------------------------- 1348 987 17646328 935 --------------G-------------------K------------------------- 936 988  4582789 865 --------------G-------------------K------------------------- 866 989  7489274 948 --------------G-------------------R------------------------- 949 990  2833389 948 --------------G-------------------R------------------------- 949 991 15221083 745 --------------G-------------------K------------------------- 746 992  4582783 584 --------------K-------------------G------------------------- 585 993 15717885 610 --------------D-------------------RPDRMRDNSHGRINAVKG-------- 628 994 15236819 724 --------------G-------------------SCGLDVNQLNRPDRMQDHSSGDRVNP 750 995 18461221 511 --------------A-------------------P------------------------- 512 996  8901183 350 --------------D-------------------K------------------------- 351 997 17227527 209 --------------K-------------------G------------------------- 210 998 16329217 183 --------------GLNNDSYYFSYDRLQDNFNPN------------------------- 203 999  2811062 202 --------------K-------------------G------------------------- 203 1000  7484399 140 --------------D-------------------K------------------------- 141 1001 18309046 208 --------------K-------------------G------------------------- 209 1002 15903076 202 --------------K-------------------A------------------------- 203 1003 17229371 181 --------------A-------------------A------------------------- 182 1004 15900991 202 --------------K-------------------A------------------------- 203 1005 16124067 175 --------------S-------------------ELHLPAEFFQIYGLEFYGQISYLKA- 200 1006 16080147 181 --------------G-------------------L------------------------- 182 1007 16273270 199 --------------K-------------------S------------------------- 200 1008 15602409 199 --------------K-------------------A------------------------- 200 1009 15672681 181 --------------G-------------------D------------------------- 182 1010 17938870 192 --------------E-------------------R------------------------- 193 1011 16119514 171 --------------E-------------------R------------------------- 172 1012 15613648 196 --------------K-------------------G------------------------- 197 1013 16331219 181 --------------A-------------------A------------------------- 182 1014 17366711 176 --------------G-------------------D------------------------- 177 1015 15805621 213 --------------M-------------------K------------------------- 214 1016 15620537 181 --------------A-------------------A------------------------- 182 1017 15641730 203 --------------SMLR----------------A------------------------- 207 1018  7489711 402 KLYDNIGGDHSNVFA-------------------A------------------------- 417 1019 15605532 197 --------------L-------------------K------------------------- 198 1020 15803938 175 --------------N-------------------DIQLPWSFFNIHGLEFNGQISFLKA- 200 1021 17367076 185 --------------M-------------------K------------------------- 186 1022 16766821 171 --------------A-------------------K------------------------- 172 1023 16762766 171 --------------A-------------------K------------------------- 172 1024 15834801 197 --------------L-------------------K------------------------- 198 1025 15966599 202 --------------K-------------------G------------------------- 203 1026 15618857 196 --------------M-------------------K------------------------- 197 1027 17366350 178 --------------M-------------------KG------------------------ 180 1028 15384987 341 RLYDPVGGEHSNVFA-------------------A------------------------- 356 1029  2129898 470 --------------A-------------------A------------------------- 471 1030  2833384 470 --------------A-------------------A------------------------- 471 1031 15028467 398 RLYDPVGGEHSNVFA-------------------A------------------------- 413 1032 15643657 201 --------------G-------------------QLNFLKG------------------- 208 983 maize-Du1 195 ---A--------------MR-----------------------------Y---------- 198 984  7489826 1395 ---A--------------MR-----------------------------Y---------- 1398 985  9502145 1332 ---A--------------MT-----------------------------Y---------- 1335 986  9502143 1349 ---A--------------MT-----------------------------Y---------- 1352 987 17646328 937 ---A--------------MA-----------------------------R---------- 940 988  4582789 867 ---A--------------MA-----------------------------Y---------- 870 989  7489274 950 ---A--------------MT-----------------------------N---------- 953 990  2833389 950 ---A--------------MT-----------------------------N---------- 953 991 15221083 747 ---A--------------MT-----------------------------F---------- 750 992  4582783 586 ---A--------------VV-----------------------------Y---------- 589 993 15717885 629 ---A--------------VV-----------------------------Y---------- 632 994 15236819 751 VKGA--------------II-----------------------------F---------- 757 995 18461221 513 ---D--------------LS-----------------------------Y---------- 516 996  8901183 352 ---A--------------LDERTIGHNPERLNLMKGGIV----------Y---------- 374 997 17227527 211 ---G--------------IV-----------------------------Y---------- 214 998 16329217 204 ---A--------------IN-----------------------------F---------- 207 999  2811062 204 ---A--------------LV-----------------------------A---------- 207 1000  7484399 142 ---A--------------LDERTIGHNPERLNLMKGGIV----------Y---------- 164 1001 18309046 210 ---A--------------IN-----------------------------Y---------- 213 1002 15903076 204 ---G--------------IL-----------------------------Y---------- 207 1003 17229371 183 ---A--------------VQ-----------------------------F---------- 186 1004 15900991 204 ---G--------------IL-----------------------------Y---------- 207 1005 16124067 201 ---G--------------LF-----------------------------F---------- 204 1006 16080147 183 ---E--------------MD-----------------------------HFHYERLECNG 196 1007 16273270 201 ---G--------------LF-----------------------------Y---------- 204 1008 15602409 201 ---G--------------LY-----------------------------Y---------- 204 1009 15672681 183 ---A--------------LSELFGMGMERYFEGVVRHNGMLNMLKTGILY---------- 215 1010 17938870 194 ---AGMLGLPSHLCTVDCLE-----------------------------Y---------- 211 1011 16119514 173 ---AGMLGLPSHLCTVDCLE-----------------------------Y---------- 190 1012 15613648 198 ---A--------------LV-----------------------------H---------- 201 1013 16331219 183 ---A--------------IQ-----------------------------F---------- 186 1013 17366711 178 ---A--------------LSELFGMGMERYFEGVVRHNGMLNMLKTGILY---------- 210 1014 15805621 215 ---AG-------------LN-----------------------------F---------- 219 1015 15620537 183 ---A--------------LL-----------------------------Y---------- 186 1016 15641730 208 ---G--------------IA-----------------------------F---------- 211 1017  7489711 418 ---G--------------LK-----------------------------T---------- 421 1018 15605532 199 ---G--------------AL-----------------------------Y---------- 202 1019 15803938 201 ---G--------------LY-----------------------------Y---------- 204 1020 17367076 187 ---AG-------------LN-----------------------------F---------- 191 1021 16766821 173 ---H--------------MDDIELPWSFFNMHGLEFNGQLSFLKAGLY-Y---------- 204 1022 16762766 173 ---H--------------MDDIELPWSFFNMHGLEFNGQLSFLKAGLY-Y---------- 204 1023 15834801 199 ---G--------------AL-----------------------------Y---------- 202 1024 15966599 204 ---G--------------LQ-----------------------------T---------- 207 1025 15618857 198 ---G--------------AL-----------------------------Y---------- 201 1026 17366350 181 ---G--------------IV-----------------------------F---------- 184 1027 15384987 357 ---G--------------LK-----------------------------M---------- 360 1028  2129898 472 ---G--------------LK-----------------------------T---------- 475 1029  2833384 472 ---G--------------LK-----------------------------T---------- 475 1030 15028467 414 ---G--------------LK-----------------------------M---------- 417 1031 15643657 209 ---G--------------IV-----------------------------F---------- 212 983 Maizedu1 199 -----------C--------------DK-------------A-----------------T 203 984  7489826 1399 -----------C--------------DK-------------A-----------------T 1403 985  9502145 1336 -----------C--------------DK-------------A-----------------T 1340 986  9502143 1353 -----------C--------------DK-------------A-----------------T 1357 987 17646328 941 -----------C--------------DK-------------A-----------------T 945 988  4582789 871 -----------A--------------DK-------------A-----------------T 875 989  7489274 954 -----------A--------------DK-------------A-----------------T 958 990  2833389 954 -----------A--------------DK-------------A-----------------T 958 991 15221083 751 -----------A--------------DK-------------A-----------------T 755 992  4582783 590 -----------S--------------NI-------------V-----------------T 594 993 15717885 633 -----------S--------------NI-------------V-----------------T 637 994 15236819 758 -----------S--------------NI-------------V-----------------T 762 995 18461221 517 -----------CGLDVEQLDRPDRMQDN-------------AHGRINVAKGGIVYSNIVT 552 996  8901183 375 -----------C--------------NA-------------V-----------------T 379 997 17227527 215 -----------S--------------NA-------------V-----------------T 219 998 16329217 208 -----------M--------------KG-------------G-----------------I 212 999  2811062 208 -----------S--------------DL-------------I-----------------T 212 1000  7484399 165 -----------C--------------NA-------------V-----------------T 169 1001 18309046 214 -----------S--------------DR-------------I-----------------L 218 1002 15903076 208 -----------A--------------NR-------------V-----------------S 212 1003 17229371 187 -----------A--------------DR-------------V-----------------N 191 1004 15900991 208 -----------A--------------NR-------------V-----------------S 212 1005 16124067 205 -----------A--------------DH-------------V-----------------T 209 1006 16080147 197 FVNFMKAGIIAA--------------DH-------------V-----------------T 212 1007 16273270 205 -----------S--------------DA-------------S-----------------T 209 1008 15602409 205 -----------S--------------DA-------------V-----------------T 209 1009 15672681 216 -----------A--------------DR-------------V-----------------N 220 1010 17938870 212 -----------Y--------------DDMSFLKGGLTTASAV-----------------T 229 1011 16119514 191 -----------Y--------------DDMSFLKGGLTTASAV-----------------T 208 1012 15613648 202 -----------S--------------DR-------------V-----------------T 206 1013 16331219 187 -----------A--------------NT-------------V-----------------T 191 1014 17366711 211 -----------A--------------DR-------------V-----------------N 215 1015 15805621 220 -----------A--------------GH-------------V-----------------T 224 1016 15620537 187 -----------A--------------DR-------------V-----------------N 191 1017 15641730 212 -----------A--------------DK-------------V-----------------N 216 1018  7489711 422 -----------A--------------DR-------------V-----------------V 426 1019 15605532 203 -----------CS-------------DF-------------V-----------------T 208 1020 15803938 205 -----------A--------------DH-------------I-----------------T 209 1021 17367076 192 -----------A--------------GH-------------V-----------------T 196 1022 16766821 205 -----------A--------------DH-------------I-----------------T 209 1023 16762766 205 -----------A--------------DH-------------I-----------------T 209 1024 15834801 203 -----------CS-------------DF-------------V-----------------T 208 1025 15966599 208 -----------A--------------SA-------------I-----------------T 212 1026 15618857 202 -----------CS-------------DY-------------I-----------------T 207 1027 17366350 185 -----------A--------------RR-------------V-----------------T 189 1028 15384987 361 -----------A--------------DR-------------A-----------------V 365 1029  2129898 476 -----------A--------------DR-------------I-----------------V 480 1030  2833384 476 -----------A--------------DR-------------I-----------------V 480 1031 15028467 418 -----------A--------------DR-------------A-----------------V 422 1032 15643657 213 -----------S--------------DV-------------I-----------------N 217 983 maize DU1 204 TVSNTYSKE----V-------S--------G-------H-------G-----A------- 218 984  7489826 1404 TVSNTYSKE----V-------S--------G-------H-------G-----A------- 1418 985  9502145 1341 TVSPTYSRD----V-------A--------G-------H-------G-----A------- 1355 986  9502143 1358 TVSPTYSRD----V-------A--------G-------H-------G-----A------- 1372 987 17646328 946 TVSYTYSRE----V-------S--------G-------H-------G-----A------- 960 988  4582789 876 TVSPTYSRE----I-------A--------G-------N-------H-----A------- 890 989  7489274 959 TVSPTYSQE----V-------S--------G-------N-------P-----V------- 973 990  2833389 959 TVSPTYSQE----V-------S--------G-------N-------P-----V------- 973 991 15221083 756 TVSPTYAKE----V-------A--------G-------N-------S-----V------- 770 992  4582783 595 TVSPTYAQE----V-------R--------TAEGGKGLH-------S-----T------- 616 993 15717885 638 TVSPTYALE----V-------R--------S-------E-------G-----GRGLQDT- 658 994 15236819 763 TVSPTYAQE----V-------R--------TAEGGKGLH-------S-----T------- 784 995 18461221 553 TVSPTYALE----V-------R--------S-------E-------G-----GRGLQDT- 573 996  8901183 380 TVSPTYANE----V-------L--------N-------G-------G-----AAGWLRST 401 997 17227527 220 TVSPNHALE----A-------QYTDVGCGLG-------H-------------T------- 241 998 16329217 213 VYSN-YVNT----V-------S--------P-------H-------H-----AWEARFSD 233 999  2811062 213 TVSPTYKEE----I-------Q--------TAYYGERLD-------G-----L------- 234 1000  7484399 170 TVSPTYANE----V-------L--------N-------G-------G-----AAGWLRST 191 1001 18309046 219 TVSETYAKE----I---------------------------------------------- 229 1002 15903076 213 TVSPSYAHE----IMT-----S--------Q-------F-------G-----C------- 229 1003 17229371 192 TVSPTYAEQ----I-------KTP------A-------Y-------G-----E------- 208 1004 15900991 213 TVSPSYAHE----IMT-----S--------Q-------F-------G-----C------- 229 1005 16124067 210 TVSPTYAKE----I-------TQPAF----G-------Y-------GMEGLLQ------- 233 1006 16080147 213 TVSPTYRNE----I---------------------------------------------- 222 1007 16273270 210 AVSPTYAQE----I-------TTPEFAY--G-------L-------Q-----G------- 230 1008 15602409 210 AVSPTYAKE----I-------TTPEF----G-------Y-------GLQGLLT------- 233 1009 15672681 221 TVSPTYAKE----I-------QTSEFGC--G-------L-------E-----S------- 241 1010 17938870 230 TVSPTYARE----ILTPEMGMG--------M-------H-------G-----V------- 251 1011 16119514 209 TVSPTYARE----ILTPEMGMG--------M-------H-------G-----V------- 230 1012 15613648 207 TVSPTYAQE----I-------Q--------TPAFGEGLH-------G-----L------- 228 1013 16331219 192 TVSPTYAQQ----I-------QTP------A-------Y-------G-----E------- 208 1014 17366711 216 TVSPTYAKE----I-------QTSEFGC--G-------L-------E-----S------- 236 1015 15805621 225 TVSPTYAQE----I-------TTPQY----G-------E-------GLEGLLV------- 248 1016 15620537 192 TVSPTYAQQ----I-------QTP------T-------Y-------G-----E------- 208 1017 15641730 217 AVSPNYAAELLTPL-------G--------A-------H-------G-----L------- 235 1018  7489711 427 TVSNGYMWE----L-------K--------TSEGGWGLH-------D-----I------- 448 1019 15605532 209 TVSPTYAKE----ILEDYSDYE--------I-------H-------D-----A------- 230 1020 15803938 210 AVSPTYARE----I-------TEPQFAY--G-------M-------E-----G------- 230 1021 17367076 197 TVSPTYAQE----I-------TTPQY----G-------E-------GLEGLLV------- 220 1022 16766821 210 AVSPTYARE----I-------TEPQFAY--G-------M-------E-----G------- 230 1023 16762766 210 AVSPTYARE----I-------TEPQFAY--G-------M-------E-----G------- 230 1024 15834801 209 TVSPTYAKE----ILQDYSDYE--------I-------H-------D-----A------- 230 1025 15966599 213 TVSPSYAQE----ILTPEFGMG--------L-------D-------G-----L------- 234 1026 15618857 208 TVSLTYVQE----I-------I--------NDYSDYELH-------D-----A------- 229 1027 17366350 190 TVRPSYAEE----I-------Q--------TPEFGMGLD-------G-----V------- 211 1028 15384987 366 TVSHCYLWE----I-------KTMDGGW--G-------L-------H-----E------- 386 1029  2129898 481 TVSHCYAWE----L-------K--------TSEGGWGLH-------N-----I------- 502 1030  2833384 481 TVSHCYAWE----L-------K--------TSEGGWGLH-------N-----I------- 502 1031 15028467 423 TVSHGYLWE----I-------KTMDGGW--G-------L-------H-----E------- 443 1032 15643657 218 TVSPTYAEE----I-------Q--------T-------EEYGEKLDG-----V------- 239 983 maize Du1 219 --------I---V--PHL-----G-K------------FYGILNGIDPDIWDP------Y 241 984  7489826 1419 --------I---V--PHL-----C-K------------FYGILNGIDPDIWDP------Y 1441 985  9502145 1356 --------I---A--PHR-----E-K------------FYGILNGIDPDIWDP------Y 1378 986  9502143 1373 --------I---A--PHR-----F-K------------FYGILNGIDPDIWDP------Y 1395 987 17646328 961 --------I---A--PHF-----S-K------------FHGIRNGIDPDIWDP------Y 983 988  4582789 891 --------V---A--THL-----H-K------------FHGIINGIDPDIWDP------F 913 989  7489274 974 --------I---A--PHL-----H-K------------FHGIVNGIDPDIWDP------L 996 990  2833389 974 --------I---A--PHL-----H-K------------FHGIVNGIDPDIWDP------L 996 991 15221083 771 --------I---S--AHL-----Y-K------------FHGIINGIDPDIWDP------Y 793 1033  7489827 1                                                    DP------Y 3 992  4582783 617 --------L---S--THS-----K-K------------FIGILNGIDTDIWNP------A 639 993 15717885 659 --------L---K--VHS-----R-K------------FLGILNGIDTDTWNP------C 681 994 15236819 785 --------L---N--FHS-----K-K------------FIGILNGIDTDSWNP------A 807 995 18461221 574 --------L---K--MHS-----R-K------------FVGILNGIDTGTWNP------S 596 996  8901183 402 F-------A---R--PELR----S-K------------FHGILNGIDCEEWNP------A 426 997 17227527 242 --------L---Y--LHK-----E-K------------FSGVLNGIDYDFWNP------E 264 998 16329217 234 ISCGLGHTL---E--IHQ-----Q-K------------FGGILNGLDYEVWNP------E 264 999  2811062 235 --------L---R--ARR-----D-D------------LLGILNGIDDEFYNP------E 257 1000  7484399 192 F-------A---R--PELR----S-K------------FHGILNGIDCEEWNP------A 216 1001 18309046 230 ------------T--PYF-----G-ENLDGLLRERGYALKGIVNGIDYDEFNP------S 263 1002 15903076 230 --------N---L--DHILKMESG-K------------VSGIVNGIDADLYNP------Q 257 1003 17229371 209 --------K---I--EGLLSFISG-K------------LSGIVNGIDTEVYDP------A 236 1004 15900991 230 --------N---L--DQILKMESG-K------------VSGIVNGIDADLYNP------Q 257 1005 16124067 234 --------A---L--ARQ-----G-R------------LTGILNGVDSDIWDP------Q 256 1006 16080147 223 --------M---T--PYY-----G-EQLEQVLQYREDDVTGILNGIDDTFYQP------K 257 1007 16273270 231 --------L---L--SGLKAQ--G-R------------LVGILNGVDENIWHP------N 256 1008 15602409 234 --------T---L--NSQ-----G-K------------LVGILNGVDDQIWHP------N 256 1009 15672681 242 --------I---L--QYVD----G-K------------VSGILNGIDYDIYNP------E 265 1010 17938870 252 --------L---A--RRR-----G-D------------LRGIVNGVDHDVWNP------A 274 1011 16119514 231 --------L---A--RRR-----G-D------------LRGIVNGVDHDVWNP------A 253 1012 15613648 229 --------L---H--QER-----G-K------------TRGILNGIDLEDFDP------K 251 1013 16331219 209 --------K---L--EGLLSYLSG-N------------LVGILNGIDTEIYNP------A 236 1014 17366711 237 --------I---L--QYVD----G-K------------VSGILNGIDYDIYNP------E 260 1015 15805621 249 --------R---L--THE-----G-R------------LSGILNGLDQDRWNP------R 271 1016 15620537 209 --------K---L--EGLLSFISG-K------------LSGILNGIDVDSYNP------A 236 1017 15641730 236 --------VDDFV--RRA-----R-D------------LHGIVNGCDYSEWNP------R 261 1018  7489711 449 --------I---N--QND-----W-K------------LQGIVNGIDMSEWNPAVDVHLH 477 1019 15605532 231 --------I---T--ARQ-----H-H------------LRGILNGIDTTIWGP------E 253 1020 15803938 231 --------L---L--QQRHRE--G-R------------LSGVLNGVDEKIWSP------E 256 1021 17367076 221 --------R---L--THE-----C-R------------LSGILNGLDQDRWNP------R 243 1022 16766821 231 --------L---LRQHHLE----G-R------------LSGILNGVDEKIWNF------E 256 1023 16762766 231 --------L---LHQRHLE----G-R------------LSGILNGVDEKIWNP------E 256 1024 15834801 231 --------I---T--ARQ-----H-H------------LKGILNGIDYTILDP------E 253 1025 15966599 235 --------L---S--SRV-----A-D------------LTGIVNGIDGETWDP------Q 257 1026 15618857 230 --------I---L--ARN-----S-V------------FSGIINGIDEDVWNP------K 252 1027 17366350 212 --------L---R--RHA-----G-K------------LRGILNGLDTEVFDP------G 234 1028 15384987 387 --------I---I--NHN-----DWK------------LQGIVNGIDMAEWNP------E 410 1029  2129898 503 --------I---N--ESD-----W-K------------FRGIVNGVDTKDWNP------Q 525 1030  2833384 503 --------I---N--ESD-----W-K------------FHGIVNGVDTKDWNP------Q 525 1031 15028467 444 --------I---I--NHN-----DWK------------LQGIVNGIDMAEWNP------E 467 1032 15643657 240 --------L---R--MHS-----K-D------------LYGILNGIDYELYNP------A 262 983 MaizeDu1 242 NDNFIP----VHYT------CE------NVVEGKHAAKRA-LQQKFGL-Q-QI--D--V- 277 984  7489826 1442 NDNFIP----VHYT------CE------NVVEGKHAAKRA-LQQKFGL-Q-QI--D--V- 1477 985  9502145 1379 TDNFIP----VFYT------CE------NVVEGKPAAKHA-LQQKFGL-Q-QT--D--V- 1414 986  9502143 1396 TDNFIP----VPYT------CE------NVVEGKHAAKRA-LQQKFGL-Q-QT--D--V- 1431 987 17646328 984 SDNFIP----VHYT------SE------NVVEGKSAAKKA-LQQRLGL-Q-QT--D--T- 1019 988  4582789 914 NDNSIP----VPYT------AE------NVVEGKRASKEA-LQQKLGL-K-KA--D--L- 949 989  7489274 997 NDKFIP----IPYT------SE------NVVEGKTAAKEA-LQHKLGL-K-QA--D--L- 1032 990  2833389 997 NDKFIP----IPYT------SE------NVVEGKTAAKEA-LQHKLGL-K-QA--D--L- 1032 991 15221083 794 NDNFIF----VPYT------SE------NVVEGKHAAKEE-LQNHLGL-K-SA--D--F- 829 1033  7489827 4 NDNFIP----VHYT------CE------NVVEGKHAAKRA-LQQKFGL-Q-QI--D--V- 39 992  4582783 640 TDPFLQ----VQYN------A-------NDLQGKSENKEA-LRRNLGL-S-SA--D--VR 675 993 15717885 682 TDRYLK----VQYN------AK------D-LQGKAANKAA-LREQLNL-A-SAYPS--Q- 718 994 15236819 808 TDPFLK----AQFN------AK------D-LQGKEENKMA-LRKQLGL-s-SA--E--SR 843 995 18461221 597 TDRFLA----VQYS------AT------D-LQGKAANKAF-LRKQLGL-Y-SE--D--AS 632 996  8901183 427 TDALLP----ANFD------AD------RPA-GKALCKEF-LQKGLGL---EV--DPRK- 462 997 17227527 265 IDRHIP----DNYS-------Q------DDFEQKLYNKKA-LRERLLL-Q-AA--D--K- 299 998 16329217 265 IDPLLA----SNFS------VK------TFGD-KAKNKQA-LRERLLL-E-TD--DK-K- 300 999  2811062 258 ADPFLT----ATYS------V-------HTRERKQLNKRA-LQRQFGL-P-EWD-D--V- 293 1000  7484399 217 TDALLP----ANFD------AD------RPA-GKALCKEF-LQKGLGL---EV--DPRK- 252 1001 18309046 264 KDSLIA----KNFS------VK-------TIEDKVLNKLA-LQKELGL-PINP--D--I- 299 1002 15903076 258 TDALLD----YHFN------QE------D-LSGKAKNKAK-LQERVGL-PVRA--D--V- 293 1003 17229371 237 NDKYIA----QTFT------AD-------TLDKRKANKIA-LQEEVGL-EVNS--N--A- 272 1004 15900991 258 TDALLD----YHFN------QE------D-LSGKAKNKAK-LQERVGL-PVRA--D--V- 293 1005 16124067 257 SDTLLP----TRYD------AE------N-LQAKAINKTH-LQTAMGL-Q-LA--EN-K- 292 1006 16080147 258 SDPYIE----AQYD------SG------DLA-CKLENKTK-LQQRMGLPE-KN--D--I- 293 1007 16273270 257 VDQYIP----HHYK------LK-------YMAGKKKNKAE-LQAYFNL-P-QD--E--S- 291 1008 15602409 257 HDAYIE----HEYK------LK-------AMTGKRKNKEA-LQAYFNLPQ-DP--D--A- 292 1009 15672681 266 NDILIP----YHFS-------E------EELSGKGQMKAE-LQKRTGL-PLNP--N--V- 301 1010 17938870 275 TDPYIL----ANFT------AA------TATR-RSLNKYA-LLQALGL-A-PT--Q--G- 309 1011 16119514 254 TDPYIL----ANFT------AA------TATR-RSLNKYA-LLQALGL-A-PT--Q--G- 288 1012 15613648 252 TDPHVT----YPYK-------H------NQME-KRKNKQV-IQRLFELPE-RK--D--I- 286 1013 16331219 237 EDRFIS----NVFD------AD------S-LDKRVKNKIA-IQEETGL-EINR--N--A- 272 1014 17366711 261 NDILIP----YHFS-------E------EELSGKGQMKAE-LQKRTGL-PLNP--N--V- 296 1015 15805621 272 TDPDIA----AY----------------SDPAGKAGAVKA-LRQEFGL-D-----D--A- 301 1016 15620537 237 TDRGXV----ANYD------RD------TLI-ARLNNRLA-LQKEMGL-EVNP--D--R- 272 1017 15641730 262 TDHYLP----ATYSDE----PE------SMRKGKALCKTA-LQEELHL-P-VT--D--V- 299 1018  7489711 478 SDDY------TNYT------FE------TLDTGKRQCKAA-LQRQLGL-QVRD--D--V- 512 1019 15605532 254 TDPNLA----KNYT------KELFETPSIFFEAKAENKKA-LYERLGL-S-LE--H--S- 295 1020 15803938 257 TDLLLA----SRYT-------R------DTLEDKAENKRQ-LQIAMGL-K-VD--DK-V- 292 1021 17367076 244 TDPDIA----AY----------------SDPAGKAGAVKA-LRQEFGL-D-----D--A- 273 1022 16766821 257 SDLLLA----SRYT-------R------DTLEEKAENKRQ-LQIAMGL-K-VN--DK-V- 292 1023 16762766 257 SDLLLA----SRYT-------R------DTLEEKAENKRQ-LQIAMGL-K-VN--DK-V- 292 1024 15834801 254 TDPHLA----KNYSKVLFEDPK------AFFEAKAENKKA-LYETLGL-S-LD--K--S- 295 1025 15966599 258 TDPHIP----AHYG-------P------GTLKRRAGNRKA-LEERFGL-E-KG--P--G- 292 1026 15618857 253 TDPALA----VQYD------ASLLSEP-DVLFTKKEENRAVLYEKLGI-S-SD--Y--F- 294 1027 17366350 235 KDPYLP----APYT------RE------D-PSGKARAKEV-FRERTGL-R-P-------- 266 1028 15384987 411 VDEHLQSDGYANYT------FE------TLDTGKKQCKEA-LQRQLGL-QVRD--D--V- 451 1029  2129898 526 FDAYLTSDGYTNYN------LK------TLQTGKRQCKAA-LQRELGL-PVRE--D--V- 566 1030  2833384 526 FDAYLTSDGYTNYN------LK------TLQTGKRQCKAA-LQRELGL-PVRE--D--V- 566 1031 15028467 468 VDEHLQSDGYANYT------FE------TLDTGKKQCKEA-LQRQLGL-QVRD--D--V- 508 1032 15643657 263 TDRYIY----VNYD------V-------NRLELKWENKVK-LQEELGL-PVNK--E--T- 298

[0409] TABLE XXXIV Maize soluble starch synthase III (Du I) “GLYTR” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id.No. Number # (start)                     Sequence                     end # 1034 MaizeDu1 278 -PVVGI-VTRLTAQKGIHLIKH-AIHRTLE-RNG-QVVLLGS-A-PDSRIQADFVNLANT 330 1035  7489826 1478 -PVVGI-VTRLTAQKGIHLIKH-AIHRTLE-RNG-QVVLLGS-A-PDSRIQADFVNLANT 1530 1036  9502145 1415 -PIVGI-ITRLTAQKGIHLIKH-AIHRTLE-SNG-QVVLLGS-A-PDHRIQGDFCRLADA 1467 1037  9502143 1432 -PIVGI-ITRLTAQKGIHLIKH-AIHRTLE-SNG-HVVLLGS-A-PDHRIQGDFCRLADA 1484 1038 17646328 1020 -PVVGI-ISRLTVQKGIHLIKH-AIYRTLE-RNG-QVVLLGS-A-PDHRIQGDFTNLASK 1072 1039  4582789 950 -PLVGV-ITRLTHQKGIHLIKH-AIWRTLE-RGG-QVVLLGS-A-PDHRIQNDFVNLANQ 1002 1040  7489274 1033 -PLVGI-ITRLTHQKGIHLIKH-AIWRTLE-RNG-QVVLLGS-A-PDPRVQNDFVNLANQ 1085 1041  2833389 1033 -PLVGI-ITRLTHQKGIHLIKH-AIWRTLE-RNG-QVVLLGS-A-PDPRVQNNFVNLANQ 1085 1042 15221083 830 -PVVGI-ITRLTHQKGIHLIKH-AIWRTLE-RNG-QVVLLGS-A-PDPRIQNDFVNLANQ 882 1043  7489827 40 -PVVGI-VTRLTAQKGIHLIKH-AIHRTLE-RNG-QVVLLGS-A-PDARIQADFVNLANK 92 1044  4582783 676 RPLVGC-ITRLVPQKGVHLIRH-AIYLTLE-LGG-QFVLLGS-S-PVPHIQREFEGIAN- 728 1045 15717885 719 -PLVGC-ITRLVAQKGVHLIRH-AIYKTAE-LGG-QFVLLGS-S-PVPEIQREFEGIAD- 770 1046 15236819 844 RPLVGC-ITRLVPQKGVHLIRH-AIYRTLE-LGG-QFVLLGS-S-PVPHIQREFEGIEQQ 897 1047 18461221 633 QPLVAC-ITRLVPQKGLHLIRH-AIYKTAE-LGG-QFVLLGS-S-PVPHIQREFEGVADQ 686 1048  8901183 463 -PLVAV-VSRLVPQKGIHLIKA-ALFRTVE-KGG-QFVLLGS-G-HSD---PAFRQLADQ 512 1049 17227527 300 -PIIAY-IGRLDNQKGVHLVHH-AIYHALN-KGA-QFVLLGS-A-TEAGINAHFRHEKQF 352 1050 16329217 301 -PMLCF-IGRLDGQKGVHLVHH-SIYYALS-QGA-QFVLLGS-A-TEPNLSKWFWHEKQH 353 1051  2811062 294 -PLIAM-VTRMTAQKGLDLVTC-VFHEMMS-EDM-QLVVLGT-G--DWRFEQFFSQMA-- 343 1052  7484399 253 -PLVAV-VSRLVPQKGIHLIKA-ALFRTVE-KGG-QFVLLGS-G-HSD---PAFRQLADG 302 1053 18309046 300 -PMISI-VSRLTNQKGCDLIVN-IANRLLQ-RNV-QLVILGT-G------DYNYENHFKG 347 1054 15903076 294 -PLVGI-VSRLTRQKGFDVVVE-SLHHILQ-EDV-QIVLLGT-G--DPAFEGAFSWFAQ- 344 1055 17229371 273 -FLIGM-VTRLVEQKGLDLVIQ-MLDRFMAYTDA-QFVLLGT-G--DRYYETQMWQLASR 325 1056 15900991 294 -PLVGI-VSRLTRQKGFDVVVE-SLHHILQ-EDV-QIVLLGT-G--DPAFEGAFSWFAQ- 344 1057 16124067 293 -PIFAV-VSRLTVQKGLDLVLE-ALPELLA-LGG-QLVVLGS-G--DATLQEAFLAAA-- 342 1058 16080147 294 -PLISM-VTRLTKQKGLDLVRR-IMHELLE-EQDIQLVVLGT-G------EREFEDYFRY 342 1059 16273270 292 -ALAFVMVTRLTEQKGVDLLIE-SADEIVK-QGG-QLMILGSGA-P--HLEQGIRELAER 344 1060 15602409 293 -LLFVM-VTRLTEQKGVDLLID-SAEEIVK-QGG-QLTILGS-G--SPHLEAGILHLAQQ 344 1061 15672681 302 -PLIGM-VSRLTNQKGFDLVLS-QLEKVLE-ENV-QIVLLGT-GFPE--IEEGFRYFSQK 353 1062 17938870 310 -PVFGV-VSRLTWQKGIDLLPH-VVPLIIE-RKG-RLIVHGE-G--DTALEDSLQALAKR 361 1063 16119514 289 -PVFGV-VSRLTWQKGIDLLPH-VVPLIIE-RKG-RLIVHGE-G--DTALEDSLQALAKR 340 1064 15613648 287 -PLIAM-VSRLVEEKGVPLLTQIAGELVTT-ENV-QLAILGT-G--DPSLEDQLHHLA-S 338 1065 16331219 273 -MVVGI-VARLVEQKGIDLVIQ-ILDRFMSYTDS-QLIILGT-G--DRHYETQLWQMASR 325 1066 17366711 297 -PLIGM-VSRLTNQKGFDLVLS-QLEKVLE-ENV-QIVLLGT-GFPE--IEEGFRYFSQK 348 1067 15805621 302 -PILAT-VSRLADQKGMDLLIT-ALPE-LV-RDW-NVVVLGG-G--DPLLEAALTGWA-- 350 1068 15620537 273 -FLIGF-VARLVEQKGIDLLLQ-ILDRFLSYSDA-QFVVLGT-G--ERYYETQLWELATR 325 1069 15641730 300 -PLFGM-VCRLTHQKGFHYLLP-ILEQFLR-NNV-QVVIVGT-G------EPEVAARLNK 347 1070  7489711 513 -PLIGF-IGRLDHQKGVDIIAD-AIHWIAG-QDV-QLVMLGT-G------RADLEDMLRR 560 1071 15605532 296 -PCVCI-ISRIAEQKGPHFMKQ-AILHALE-NAY-TLIIIGT-C-YGNQLHEEFANLQES 348 1072 15803938 293 -PLFAV-VSRLTSQKGLDLVLE-ALPGLLE-QGG-GLALLG--A-GDPVLQEGFLAAAAE 344 1073 17367076 274 -PILAT-VSRLADQKGMDLLIT-ALPE-LV-RDW-NVVVLGG-G--DPLLEAALTGWA-- 322 1074 16766821 293 -PLFAV-VSRLTNQKGLDLVLE-ALPGLLE-QGG-QLALLG--A-GDPVLQEGFLAAA-- 342 1075 16762766 293 -PLFAV-VSRLTNQKGLDLVLE-ALPGLLE-QGG-QLALLG--A-GDPVLQEGFLAAA-- 342 1076 15834801 296 -PCMCI-ISRIAEQKGPEFMKQ-AILHALE-NAY-TLIIIGT-C-YGGQIHKEFSNLQES 348 1077 15966599 293 -PIFCV-ISRLTWQKGMDLVAE-AADDIVA-LGG-KLVVLGS-G--DPALESALMAAASR 344 1078 15618857 295 -PLICV-ISRIVEEKGPEFMKE-IILHAME-HSY-AFILIGT-S-QNEVLLNEFRNLQDC 347 1079 17366350 267 -PVLAY-VGRLDYQKGLDLVLK-ALPRLLE-MGF-RLYVQGV-G--DGGLQEAFLRAEEE 318 1080 15384987 452 -PLIGF-IGRLDHQKGVDIIGD-AMPWIAG-QDV-QVVMLGT-G------RPDLEEMLRR 499 1081  2129898 567 -PIISF-IGRLDHQKGVDLIAE-AIPWMMS-HDV-QLVMLGT-G------RADLEQMLKE 614 1082  2833384 567 -PIISF-IGRLDHQKGVDLIAE-AIPWMMS-HDV-QLVMLGT-G------RADLEQMLKE 614 1083 15028467 509 -PLIGF-IGRLDHQKGVDIIGD-AMPWIAG-QDV-QVVMLGT-G------RPDLEEMLRR 556 1084 15643657 299 -AVAGL-ISRLVPQKGLDLLVD-VMDYLTL-FDL-QIVVLGT-G-DEQ-----YENAFRK 346 1034 Maize DU1 331 LHGVNHGQVRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTQLVAMRYGTIPIVRKTGG 390 1035  7489826 1531 LHGVNHGQVRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTQLVAMRYGTIPIVRKTGG 1590 1036  9502145 1468 LHGVYHGRVKLVLTYDEPLSHLIYAGSDFIIVPSIFEPCGLTQLVAMRYGSIPIVRKTGG 1527 1037  9502143 1485 LHGVYHGRVKLVLTYDEPLSHLIYAGSDFIIVPSIFEPCGLTQLVAMRYGSIPIVRKTGG 1544 1038 17646328 1073 LHGEYHGRVKLCLTYDEPLSHLIYAGADFILVPSMFEPCGLTQLTAMRYGSIPIVRKTGG 1132 1039  4582789 1003 LHSSHNDRARLCLAYDEPLSHMIYAGADFILVPSIFEPCGLTQLTAMRYGSIPIVRKTGG 1062 1040  7489274 1086 LHSKYNDRARLCLTYDEPLSHLIYAGADFILVPSIFEPCGLTQLTAMRYGSIPVVRKTGG 1145 1041  2833389 1086 LHSKYNDRARLCLTYDEPLSHLIYAGADFILVPSIFEPCGLTQLTAMRYGSIPVVRKTGG 1145 1042 15221083 883 LHSSHGDRARLVLTYDEPLSHLIYAGADFILVPSIFEPCGLTQLIAMRYGAVPVVRKTGG 942 1043  7489827 93 LHGVNHGQCRLSLTYDEPLSHLIYAGSDFILVPSIFEPCGLTHLVAMRYGTIPIVRKTGG 152 1044  4582783 729 -HFQNHDHIRLILKYDESLSHAIYAASDMFIIPSIFEPCGLTQMISMRYGAIPIARKTGG 787 1045 15717885 771 -HFQNNNNIRLILKYDDALSHCIYAASDMFIVPSIFEPCGLTQMIAMRYGSVPIVRKTGG 829 1046 15236819 898 FK--SHDHVRLLLKYDEALSHTIYAASDLFIIPSIFEPCGLTQMIAMRYGSIPIARKTGG 955 1047 18461221 687 FQKNNN--IRLILKYDEALSHCIYAASDMFIIPSMFEPCGLTQMIAMRYGSVPIVRQTGG 744 1048  8901183 513 QFK-DHPNCRLKIMYSERLAHMIYAAADVVVVPSMFEPCGLTQMIALRYGAVPLVRRTGG 571 1049 17227527 353 LN--SNPDVHLELGFNEELSHLIYAGADMIVVPSNYEPCGLTQMIGLKYGTVPIVRGVGG 410 1050 16329217 354 LN--DNPNVHLELGFDEELAHLIYGAADIIVVPSNYEPCGLTQMIGLRYGAVPVVRGVGG 411 1051  2811062 344 --AAYPGKVGVYIGFHEPLAHQIYAGADLFLIPSLFEPCGLSQMIALRYGTIPIVRETGG 401 1052  7484399 303 QFK-DHPNCRLKIMYSERLAHMIYAAADVVVVPSMFEPCGLTQMIALRYGAVPLVRRTGG 361 1053 18309046 348 LQELYPTKVSANIKFDNGLAHRIYASSDIFLMPSLFEPCGLGQLIALRYGAIPIVRETGG 407 1054 15903076 345 ---IYPDKLSTNITFDVKLAQEIYAACDLFLMPSRFEPCGLSQMMAMRYGTLPLVHEVGG 401 1055 17229371 326 Y----PGRMATYLLYNDALSRRIYAGTDAFLMPSRFEPCGISQMMALRYGSIPIVRRTGG 381 1056 15900991 345 ---IYPDKLSTNITFDVKLAQEIYAACDLFLMPSRFEPCGLSQMMAMRYGTLPLVHEVGG 401 1057 16124067 343 --AEHSGQVGVQIGYHEAFSHRIIAGSDVILVPSRFEPCGLTQLYGLKYGTLPLVRHTGG 400 1058 16080147 343 AEFAFHEKCRAYIGFDEPLAHQIYAGSDMFLMPSKFEPCGLGQLIALQYGAIPIVRETGG 402 1059 16273270 345 Y----PQNIAVKIGYDEALSHLMVAGGDVILVPSRFEPCGLTQLYGLQYGTLPLVRKTGG 400 1060 15602409 345 Y----PHQIAVKIGYDEALSHLMIAGGDVILVPSRFEPCGLTQLYGLKYGTLPLVRATGG 400 1061 15672681 354 Y----PDKLSANIAFDIQFAQEIYAGSDFFLMPSAFEPCGLSQMIAMRYGTLPIVHEIGG 409 1062 17938870 362 YPEL----VCAHIGYDERLAHMIQAGSDFIIQPSRFEPCGLTQLYLARYGALPIVSRTGG 417 1063 16119514 341 YPEL----VCAHIGYDERLAHMIQAGSDFIIQPSRFEPCGLTQLYALRYGALPIVSRTGG 396 1064 15613648 339 LHP---HQISFKCVFAEPLARKLYAGADLFIMPSRFEPCGLSQMISLRYETVPIVRETGG 395 1065 16331219 326 F----PGRMAVQLLHNDALSRRVYAGADVFLMPSRFEPCGLSQLMAMRYGCIPIVRRTGG 381 1066 17366711 349 Y----PDKLSANIAFDIQFAQEIYAGSDFFLMPSAFEPCGLSQMIAMRYGTLPIVHEIGG 404 1067 15805621 351 ----NHPRVAFASGMNEPLAHRIYAGAHAFAMPSRFEPCGLSQLIAMRYGTLPIVRETGG 406 1068 15620537 326 Y----PGRMSTYLMYDEGLSRRIYAGSDAFLVPSRFEPCGITQMLALRYGSVPIVRRTGG 381 1069 15641730 348 IAHYHRAKFAFVETYSERLAHWVEAGSDFFLMPSEFEACGLNQIYSMAYGTLPIVREVGG 407 1070  7489711 561 FESEHSDKVRAWVGFSVPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 620 1071 15605532 349 L--ANSPDVRILLTYSDVLARQIFAAADMICIPSMFEPCGLTQMIGMRYGTVPLVRATGG 406 1072 15803938 345 Y----PGQVGVQIGYHEAFSHRIMGGADVILVPSRFEPCGLTQLYGLKYGTLPLVRRTGG 400 1073 17367076 323 ----NHPRVAFASGMNEPLAHRIYAGAHAFAMPSRFEPCGLSQLIAMRYGTLPIVRETGG 378 1074 16766821 343 --AEHPGQVGVQIGYHEAFSHRIMGGADVILVPSRFEPCGLTQLYGLKYGTLPLVRRTGG 400 1075 16762766 343 --AEHPGQAGVQIGYHEAFSHRIMGGADVILVPSRFEPCGLTQLYGLKYGTLPLVRRTGG 400 1076 15834801 349 L--ADSPNVRILLTYSDVLARQIFAAADMICIPSMFEPCGLTQMIGMRYGTVPVVRATGG 406 1077 15966599 345 ----NRGHIGMVTGYDEPLSHLMQAGADAILIPSRFEPCGLTQLYGLRYGCVPVVARTGG 400 1078 15618857 348 L--ASSPNIRLILDFNDPLARLTYAAADMICIPSHREACGLTQLIAMRYGTVPLVRKTGG 405 1079 17366350 319 ----NPEGVRFLPAYDEAMARLAYAGAEAVLVPSRFEPCGLVQMIASRYGTPPVARAVGG 374 1080 15384987 500 FESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYGTVPVVHAVGG 559 1081  2129898 615 FEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVGG 674 1082  2833384 615 FEAQHCDKIRSWVGFSVKMAHRITAGSDILLMPSRFEPCGLNQLYAMSYGTVPVVHGVGG 674 1083 15028467 557 FESEHNDKVRGWVGFSVQLAHRITAGADVLLMPSRFEPCGLNQLYAMAYSTVPVVHAVGG 616 1084 15643657 347 FQERYPDKVSANIKFDVELAQKIYAGADIFLMPSRYEPCGLGQMFSMRYGTIPVVRYTGG 406 1034 MaizeDu1 391 LFDTV--FD--VDNDKERARDRGLE---P-----N-GFS-FDGA-DS------------- 422 1035  7489826 1591 LFDTV--FD--VDNDKERARDRGLE---P-----N-GFS-FDGA-DS------------- 1622 1036  9502145 1528 LYDTV--FD--VDNDKDRARSLGLE---P-----N-GFS-FDGA-DS------------- 1559 1037  9502143 1545 LHDTV--FD--VDNDKDRARSLGLE---P-----N-GFS-FDGA-DS------------- 1576 1038 17646328 1133 LYDTV--FD--VDDDKDRAREQGLE---P-----N-GFS-FEGA-DS------------- 1164 1039  4582789 1063 LYDTV--FD--VDNDKDRAQVQGLE---P-----N-GFS-FDGA-DA------------- 1094 1040  7489274 1146 LYDTV--FD--VDHDKERAQQCGLE---P-----N-GFS-FDGA-DA------------- 1177 1041  2833389 1146 LYDTV--FD--VDHDKERAQQCGLE---P-----N-GFS-FDGA-DA------------- 1177 1042 15221083 943 LFDTV--FD--VDHDKERAQAQVLE---P-----N-GFS-FDGA-DA------------- 974 1043  7489827 153 LFDTV--FD--VDNDKERARDRGLE---P-----N-GFS-FDGA-DS------------- 184 1044  4582783 788 LNDSV--FD--VDDDTIPSQFR------------N-GFT-FLNA-DE------------- 815 1045 15717885 830 LNDSV--FD--FDDETIPMEVR------------N-GFT-FVKA-DE------------- 857 1046 15236819 956 LNDSV--FD--IDDDTIPTQFQ------------N-GFT-FQTA-DEQLKIGMEIYLVWF 996 1047 18461221 745 LCDSV--FD--FDDETIPVELR------------N-GFT-FART-DE------------- 772 1048  8901183 572 LADTV--FD--VDGP---AGGPAQP---R-----N-GFV-FDGS-DD------------- 600 1049 17227527 411 LVNTV--FD--RDYDQNLPPEK------R-----N-GYV-FYQS-DN------------- 439 1050 16329217 412 LVNTV--FD--RDYDQNHPPEK------R-----N-GFV-FYQP-DE------------- 440 1051  2811062 402 LNDTV-----------QSYNEITKE---G-----N-GFS-FTNF-NA------------- 426 1052  7484399 362 LADTV--FD--VDGP---AGGPAQP---R-----N-GFV-FDGS-DD------------- 390 1053 18309046 408 LKDTI--HS--YN------KYTGI----G-----N-GFS-FTNY-NH------------- 432 1054 15903076 402 LRDTV----------------RAFN---PIEGSGT-GFS-FDNL-SP------------- 426 1055 17229371 382 LVDTV--SH--HDPINEAG---------------T-GYC-FDRY-EP------------- 406 1056 15900991 402 LRDTV----------------RAFN---PIEGSGT-GFS-FDNL-SP------------- 426 1057 16124067 401 LADTV------VDCALENLADG--S---A-----S-GFV-FNEC-EA------------- 428 1058 16080147 403 LYDTV--RA--YQEEEGTG---------------N-GFT-FSAF-NA------------- 427 1059 16273270 401 LADTV--VD--STSESIKAR----T---A-----T-GFV-FESA-TP------------- 428 1060 15602409 401 LADTV--VNATVENIKSRL---------A-----T-GFV-FEQA-NR------------- 428 1061 15672681 410 LKDTV--IP--FNPISK-------E---G-----T-GFG-FVDF-EG------------- 434 1062 17938870 418 LAETI--ID---------ANDAAIEAGVA-----T-GFQ-FEPA-NE------------- 445 1063 16119514 397 LAETI--ID---------ANDAAIEAGVA-----T-GFQ-FEPA-NE------------- 424 1064 15613648 396 LYDTI--QS--YNEEIG-------E---G-----N-GFS-FTHY-NA------------- 420 1065 16331219 382 LVDTV--SF--YDPINEAG---------------T-GYC-FDRY-EP------------- 406 1066 17366711 405 LKDTV--IP--FNPISK-------E---G-----T-GFG-FVDF-EG------------- 429 1067 15805621 407 LADTV-------------------P---P-----EVGFR-FADA-TA------------- 424 1068 15620537 382 LVDTV--FH--HD-------PRHAE---G-----N-GYC-FDRY-EP------------- 406 1069 15641730 408 LKDTV--ND--YDKFPERA---------------T-GFG-YQEP-TP------------- 432 1070  7489711 621 LRDTVAPFD--PFNDT------GL------------GWT-FDRA-EA------------- 645 1071 15605532 407 LADTV--AN-------------GI----------N-GFSFFNPH-DF------------- 426 1072 15803938 401 LADTV--SD--C--SLENLAD-GV----A-----S-GFV-FEDS-NA------------- 428 1073 17367076 379 LADTV-------------------P---P-----EVGFR-FADA-TA------------- 396 1074 16766821 401 LADTV------SDSSLENLAD-GI----A-----S-GFV-FEDS-NA------------- 428 1075 16762766 401 LADTV------SDSSLENLAD-GI----A-----S-GFV-FEDS-NA------------- 428 1076 15824801 407 LADTV--TD-------------GV----------N-GFS-FSNPHDF------------- 426 1077 15966599 401 LTDTI--ID--ANEAALSAKC-------A-----T-GFH-FLPV-TT------------- 428 1078 15618857 406 LADTV--IP-------------GV----------N-GFTFFDTN-NF------------- 425 1079 17366350 375 LKDTV--ED-------GRA-----------------GVL-FETY-HP------------- 393 1080 15384987 560 LRDTV--AP--FDP----FADTGL------------GWT-FDRA-EA------------- 584 1081  2129898 675 LRDTV--QP--FNPFDESGV----------------GWT-FDRA-EA------------- 699 1082  2833384 675 LRDTV--QP--FNPFDESGV----------------GWT-FDRA-EA------------- 699 1083 15028467 617 LRDTV--AP--FDP----FADTGL------------GWT-FDRA-EA------------- 641 1084 15643657 407 LADTV--KE--YD-------PQSME---G-----T-GFG-FKKY-DS------------- 431

[0410] TABLE XXXV Maize soluble starch synthase III (Du I) “CTEND” Domain Alignments with other similar proteins SEQ Accession a.a a.a. Id. No. Number # (start) Sequence end # 1085 MaizeDu1 423  ---------------NGVDYALNRAISAW--F-DARSWFHSLCKRVMEQDWSWNRPALDY 464 1086 7489826 1623 ---------------NGVDYALNRAISAW--F-DARSWFHSLCKRVMEQDWSWNRPALDY 1664 1087 9502145 1560 ---------------NGVDYALNRAIGAW--F-DARSWFHSLCKRVMEQDWSWNRPALDY 1601 1088 9502143 1577 ---------------NGVDYALNRAIGAW--F-DARSWFHSLCKRVMEQDWSWNRPALDY 1618 1089 17646328 1065 ---------------NGVDYALDRAITTW--Y-DARSWFHSLCKRVMEQDWTWNRPALDY 1206 1090 4582789 1095 ---------------GGVDYALNRAISAW--Y-DGREWFNTLCKTVMEQDWSWNRPALDY 1136 1091 7489274 1178 ---------------GGVDYALNRALSAW--Y-DGRDWFNSLCKQVMEQDWSWNRPALDY 1219 1092 2833389 1178 ---------------GGVDYALNRALSAW--Y-DGRDWFNSLCKQVMEQDWSWNRPALDY 1219 1093 15221083 975 ---------------PGVDYALNRAISAW--Y-DGREWFNSLCKTVMEQDWSWNRPALEY 1016 1094 7489827 185 ---------------NGVDYALNRAISAW--F-DARSWFHSLCKRVMEQDWSWNRPALDY 226 1095 4582783 816 ---------------KGINDALVRAINLF--TNDPKSW-KQLVQKDMNIDFSWDSSAAQY 857 1096 15717885 858 ---------------QGLSSAMERAFNCY--T-RKPEVWKQLVQKDMTIDFSWDTSASQY 899 1097 15236819 997 SFTCPSLAEKGNVKKQGFNYALERAFNHY--K-KDEEKWMRLVEKVMSIDFSWGSSATQY 1053 1098 18461221 773 ---------------QDLSSCLERAFSYY--S-RKPMVWKQLVQKDMQIDFSWDSPASQY 814 1099 8901183 601 ---------------GALHGALDRALTLY--T-TQPERWAALQQDNMRLDVSWGKSAKSY 642 1100 17227527 440 ---------------QALESAMNRAIDLW--Y-QSPEQFQQLAIQGMKYDYSWNNPGTEY 481 1101 16329217 441 ---------------YALETALSRAIALY--K-DDPVAFKTLALQGMAYDYSWNKPGLQY 482 1102 2811062 427 ---------------HDMLYTIRRALSFY--R-QPSVW-EQLTERAMRGDYSWRRSANQY 467 1103 7484399 391 ---------------GALHGALDRALTLY--T-TQPERWAALQQDNMRLDVSWGKSAKSY 432 1104 18309046 433 ---------------NDLMHVIELALETY--D-DKEIW-RSLIIQAMDSDNSWNKSAEKY 473 1105 15903076 427 ---------------YWLNWTFQTALDLY--R-NHPDIWRNLQKQAMESDFSWDTACKSY 468 1106 17229371 407 ---------------LDLFTCM---IRAWEGF-RYKPQWQELQKRGMSQDFSWYKSAKEY 447 1107 15900991 427 ---------------YWLNWTFQTALDLY--R-NHPDIWRNLQKQAMESDFSWDTACKSY 468 1108 16124067 429 ---------------QALVKAIRRAFVLW--S-RPKHWRH-VQRHAMRLDFGWQLAAVDY 469 1109 16080147 428 ---------------HDLKFTIERALSFY--C-QQDVW-KSIVKTAMNADYSWGKSAKEY 468 1110 16273270 429 ---------------EALRHCLQRAFALW--Q-KPRAW-AMVRTDAMEQDFSWRKAAEQY 469 1111 15602409 429 ---------------EALRQALVNAFALW--Q-KQRLWF-TVRSVAMEQDFSWQISATGY 469 1112 15672681 435 ---------------QILVETINRALEVY--G-KEPEVLNKMVLSAMSKDFSWGTKAQQY 476 1113 17938870 446 ---------------DDLRAALERAISAY--N-D-RELFRRLQTQAMQANFSWDKSAAQY 486 1114 16119514 425 ---------------DDLRAALERAISAY--N-D-RELFRRLQTQAMQANFSWDKSAAQY 465 1115 15613648 421 ---------------HDFLYTIKRALRFY--R-TEKEW-ENLLLNIYSSEVGWDVSAKQY 461 1116 16331219 407 ---------------LDCFTAMVRAWEGF--R-FKADW-QKLQQRAMRADFSWYRSAGEY 447 1117 17366711 430 ---------------QILVETINRALEVY--G-KEPEVLNKMVLSAMSKDFSWGTKAQQY 471 1118 15805621 425 ---------------PAFLQACREAQAAF--Q-DPAQW-QTRATRAMSLDFSWDGPARQY 465 1119 15620537 407 ---------------LDLYTCLVRAWESY--Q-YQPQW-QKLQQRGMAVDLSWKQSGIAY 447 1120 15641730 433 ---------------EALLITMQRALLFY--L-QQPEEMLKVQQRAMQQNFSWEESAQEY 474 1121 7489711 646 ---------------NRMIDALSHCLTTY--R-NYKESWRACRARGMAEDLSWDHAAVLY 687 1122 15605532 427 ---------------YEFRNMLSEAVTTY--R-TNHDKWQHIVRACLDFSSDLETAANKY 468 1123 15803938 429 ---------------WSLLRAIRRAFVLW--S-RPSLW-RFVQRQAMAMDFSWQVAAKSY 469 1124 17367076 397 ---------------PAFLQACREAQAAF--Q-DPAQW-QTRATRAMSLDFSWDGPARQY 437 1125 16766821 429 ---------------WSLLRAIRRAFVLW--S-RPSLW-RFVQRQAMAMDFSWQVAAKSY 469 1126 16762766 429 ---------------WSLLRAIRRAFVLW--S-RPSLW-RFVQRQAMAMDFSWQVAAKSY 469 1127 15834801 427 ---------------HEFRNMLSKAIATY--R-DDQDKWQQIVRSCLEFSSDLETAANKY 468 1128 15966599 429 ---------------DGLRLAIRRVLRAY--N-EPKLW-ARLQYQGMKSDVSWAKSAERY 469 1129 15618857 426 ---------------NEFRAMLSNAVTTY--R-QEPDVWLNLIESGMLRASGLDAMAKHY 467 1130 17366350 394 ---------------EGLLYGVLRLF---------RLGAEEMGLRAMEKDFSWEGPARAY 429 1131 15384987 585 ---------------NRMIDALGHCLNTY--R-NYKESWRGLQARGMAQDLSWDHAA--- 623 1132 2129898 700 ---------------NKLMAALWNCLLTY--K-DYKKSWEGIQERGMSQDLSWDNAAQQY 741 1133 2833384 700 ---------------NKLMAALWNCLLTY--K-DYKKSWEGIQERGMSQDLSWDNAAQQY 741 1134 15028467 642 ---------------NRMIDALGHCLNTY--R-NYKESWRGLQARGMAQDLSWDHAA--- 680 1135 15643657 432 ---------------AHLLKAVSKALHFY--Y-REKDHWRRIMTNAMNTDLSWDRSAKEY 473 1085 MaizeDu1 465  IELY-RSASKL 474 1086 7489826 1665 IELY-RSASKL 1674 1087 9502145 1602 IELY-HAARK 1610 1088 9502143 1619 IELY-HAARK 1627 1089 17646328 1207 MELY-HSARK 1215 1090 4582789 1137 LELY-HAACKL 1146 1091 7489274 1220 LELY-HAARKL 1229 1092 2833389 1220 LELY-HAARKL 1229 1093 15221083 1017 LELY-HSARK 1025 1094 7489827 227 IELY-RSASQI 236 1095 4582783 858 EELY 861 1096 15717885 900 EDIY-Q 904 1097 15236819 1054 EELYTRSVSR 1063 1098 18461221 815 ENLY-QSA 821 1099 8901183 643 VDVY-RSIS 650 1100 17227527 482 LNIY 485 1101 16329217 483 VEAY 486 1102 2811062 468 KQAY-EQLIK 476 1103 7484399 433 VDVY-RSIS 440 1104 18309046 474 KELY-EELIK 482 1105 15903076 469 LDLY-HS 474 1106 17229371 448 DKLY-RS 453 1107 15900991 469 LDLY-HS 474 1108 16124067 470 LSLY-R 474 1109 16080147 469 QRIF-EQVTR 477 1110 16273270 470 RTLY 473 1111 15602409 470 HALY-Q 474 1112 15672681 477 IELY-Q 481 1113 17938870 487 MALF-ES 492 1114 16119514 466 MALF-ES 471 1115 15613648 462 TALY 465 1116 16331219 448 IKVY-K 452 1117 17366711 472 IELY-Q 476 1118 15805621 466 LELY-R 470 1119 15620537 448 KQLY-AEA 454 1120 15641730 475 MKMY-RLA 481 1122 15605532 469 LEIY-K 473 1123 15803938 470 RELY 473 1124 17367076 438 LELY-R 442 1125 16766821 470 RELY 473 1126 16762766 470 RELY 473 1127 15834801 469 LEIY-Q 473 1128 15966599 470 VSLY 473 1129 15618857 468 VNLY-QS 473 1130 17366350 430 REVY-REA 436 1131 15384987 624 -ELY 626 1132 2129898 742 EEVL-VAA 748 1133 2833384 742 EEVL-VAA 748 1134 15028467 681 -ELY 683 1135 15643657 474 VDLY-KKA 480

[0411] TABLE XXXVI Identities of the Accession Numbers used in Tables. XXXI-XXXIV. Accession Brief Description of sequences score Id. producing significant alignments (bits) E-value gi|7489826|pir||T01265 starch synthase DULL1 - maize >gi|30 . . . 969 0.0 gi|9502145|gb|AAF88000.1| (AF258609) starch synthase III [A . . . 815 0.0 gi|9502143|gb|AAF87999.1|AF258608_1 (AF258608) starch synth . . . 811 0.0 gi|17646328|gb|AAL40942.1|AF432915_1 (AF432915) putative st . . . 808 0.0 gi|4582789|emb|CAB40374.1| (AJ225088) Starch synthase isofo . . . 758 0.0 gi|7489274|pir|T07663 soluble starch synthase (EC 2.4.1. - ) . . . 752 0.0 gi|2833389|sp|Q43846|UGS4_SOLTU Soluble glycogen [starch] s . . . 749 0.0 gi|15221083|ref|NP_172637.1| (NM_101044) putative glycogen . . . 734 0.0 gi|7489827|pir|T01266 starch synthase DULL1 - maize (fragm . . . 495  e−139 gi|4582783|emb|CAB40375.1| (AJ006752) starch synthase, isof . . . 394  e−108 gi|15717885|gb|AAK97773.1| (AY044844) starch synthase isofo . . . 363 2e−99 gi|15236819|ref|NP_193558.1| (NM_117934) starch synthase-li . . . 361 1e−98 gi|18461221|dbj|BAB84418.1| (AP003292) putative starch synt . . . 337 2e−91 gi|8901183|gb|AAC17971.2| (AF026422) soluble starch synthas . . . 303 4e−81 gi|17227527|ref|NP_484075.1| (NC_003272) glycogen (starch) . . . 300 2e−80 gi|16329217|ref|NP_439945.1| (NC_000911) glycogen (starch) . . . 265 9e−70 gi|2811062|sp|O08328|GLGA_BACST Glycogen synthase (Starch [. . . 249 6e−65 gi|7484399|pir||T07926 probable starch synthase (EC 2.4.1.- . . . 232 5e−60 gi|18309046|ref|NP_560980.1| (NC_003366) glycogen synthase . . . 226 5e−58 gi|15903076|ref|NP_358626.1| (NC_003098) Glycogen synthase . . . 224 2e−57 gi|17229371|ref|NP_485919.1| (NC_003272) glycogen synthase . . . 222 8e−57 gi|15900991|ref|NP_345595.1| (NC_003028) glycogen synthase . . . 221 9e−57 gi|16124067|ref|NP_407380.1| (NC_003143) glycogen synthase . . . 220 2e−56 gi|16080147|ref|NP_390973.1| (NC_000964) starch (bacterial . . . 215 6e−55 gi|16273270|ref|NP_439511.1| (NC_000907) glycogen synthase . . . 214 1e−54 gi|15602409|ref|NP_245481.1| (NC_002663) GlgA [Pasteurella . . . 214 1e−54 gi|15672681|ref|NP_266855.1| (NC_002662) glycogen synthase . . . 212 8e−54 gi|17938870|ref|NP_535658.1| (NC_003306) glycogen synthase . . . 211 1e−53 gi|16119514|ref|NP_396220.1| (NC_003064) AGR_pAT_410p [Agro . . . 211 1e−53 gi|15613648|ref|NP_241951.1| (NC_002570) starch (bacterial . . . 209 4e−53 gi|16331219|ref|NP_441947.1| (NC_000911) glycogen synthase . . . 209 4e−53 gi|17366711|sp|Q9CHM9|GLGA_LACLA Glycogen synthase (Starch . . . 209 5e−53 gi|15805621|ref|NP_294317.1| (NC_001263) glycogen synthase . . . 200 3e−50 gi|15620537|gb|AAL03921.1|U30252_9 (U30252) GlgA [Synechoco . . . 199 4e−50 gi|15641730|ref|NP_231362.1| (NC_002505) glycogen synthase . . . 199 5e−50 gi|7489711|pir|T01209 ADPglucose - starch glucosyltransfera . . . 197 2e−49 gi|15605532|ref|NP_220318.1| (NC_000117) Glycogen Synthase . . . 197 2e−49 gi|15803938|ref|NP_289974.1| (NC_002655) glycogen synthase . . . 197 2e−49 gi|17367076|sp|Q9RWS1|GLGA_DEIRA Glycogen synthase (Starch . . . 197 3e−49 gi|16766821|ref|NP_462436.1| (NC_003197) glycogen synthase . . . 196 6e−49 gi|16762766|ref|NP_458383.1| (NC_003198) glycogen synthase . . . 194 2e−48 gi|15834801|ref|NP_296560.1| (NC_002620) glycogen synthase . . . 191 2e−47 gi|15966599|ref|NP_386952.1| (NC_003047) PROBABLE GLYCOGEN . . . 189 4e−47 gi|15618857|ref|NP_225143.1| (NC_000922) Glycogen Synthase . . . 189 5e−47 gi|17366350|sp|P58395|GLGA_THECA Glycogen synthase (Starch . . . 187 1e−46 gi|15384987|emb|CAC59826.1| (AJ308110) soluble starch synth . . . 187 2e−46 gi|2129898|pir||S61505 UDPglucose - starch glucosyltransfera . . . 185 9e−46 gi|2833384|sp|Q43093|UGS3_PEA Glycogen [starch] synthase, c . . . 185 1e−45 gi|15028467|gb|AAK81729.1|AF395537_1 (AF395537) soluble sta . . . 185 1e−45 gi|15643657|ref|NP_228703.1| (NC_000853) glycogen synthase . . . 184 2e−45 gi|15232051|ref|NP_186767.1| (NM_110984) putative glycogen . . . 181 1e−44 gi|13476305|ref|NP_107875.1| (NC_002678) glycogen synthase . . . 181 2e−44 gi|7489710|pir||T01208 ADPglucose - starch glucosyltransfera . . . 179 6e−44 gi|146139|gb|AAA23870.1| (J02616) glycogen synthase (EC 2.4 . . . 179 6e−44 gi|14279432|gb|AAK58596.1|AF268969_2 (AF268969) glycogen sy . . . 179 7e−44 gi|15890897|ref|NP_356569.1| (NC_003063) AGR_L_1562p [Agrob . . . 176 4e−43 gi|17366749|sp|Q9EUT5|GLGA_RHITR Glycogen synthase (Starch . . . 175 7e−43 gi|16265159|ref|NP_437951.1| (NC_003078) putative glycogen . . . 175 1e−42 gi|15895507|ref|NP_348856.1| (NC_003030) Glycogen synthase, . . . 175 1e−42 gi|14495348|gb|AAK64284.1|AF383878_1 (AF383878) soluble sta . . . 173 4e−42 gi|15606118|ref|NP_213495.1| (NC_000918) glycogen synthase . . . 173 4e−42 gi|7489695|pir||T06798 probable starch synthase (EC 2.4.1.- . . . 170 3e−41 gi|16265834|gb|AAL16661.1|AF419099_1 (AF419099) putative so . . . 169 6e−41 gi|8708896|gb|AAC17970.2| (AF026421) soluble starch synthas . . . 167 2e−40 gi|6467503|gb|AAF13168.1|AF173900_1 (AF173900) granule boun . . . 166 3e−40 gi|7529653|emb|CAB86618.1| (AJ269502) starch synthase IIa-1 . . . 162 5e−39 gi|3192881|gb|AAC19119.1| (AF068834) starch synthase [Ipomo . . . 162 6e−39 gi|8953571|emb|CAB96626.1| (AJ269503) starch synthase IIa-2 . . . 161 2e−38 gi|8953573|emb|CAB96627.1| (AJ269504) starch synthase IIa-3 . . . 159 4e−38 gi|5825480|gb|AAD53263.1|AF155217_1 (AF155217) starch synth . . . 159 6e−38 gi|15237934|ref|NP_197818.1| (NM_122336) soluble starch syn . . . 159 8e−38 gi|2833390|sp|Q43847|UGS3_SOLTU Glycogen [starch] synthase, . . . 158 1e−37 gi|6690399|gb|AAF24126.1|AF121673_1 (AF121673) soluble star . . . 157 3e−37 gi|1549232|dbj|BAA07396.1| (D38221) SSS1 [Oryza sativa] >gi . . . 156 4e−37 gi|5295947|dbj|BAA81848.1| (AB026295) ESTs AU075322(C11109) . . . 156 4e−37 gi|2833377|sp|Q40739|UGS2_ORYSA Soluble glycogen [starch] s . . . 156 4e−37 gi|5834407|gb|AAD53959.1|AF181035_3 (AF181035) glycogen syn . . . 154 2e−36 gi|17367070|sp|QPRNH6|GLGA_RHOSH Glycogen synthase (Starch . . . 154 2e−36 gi|82478|pir||JQ0703 UDPglucose - starch glucosyltransferase . . . 154 2e−36 gi|15223331|ref|NP_174566.1| (NM_103023) starch synthase, p . . . 152 8e−36 gi|2833382|sp|Q42968|UGST_ORYGL Granule-bound glycogen [sta . . . 152 8e−36 gi|15983795|gb|AAL10494.1| (AY056803) At1g32900/F9L11_8 [Ar . . . 150 2e−35 gi|7489712|pir||T01414 ADPglucose - starch glucosyltransfera . . . 150 2e−35 gi|297424|emb|CAA46294.1| (X65183) glycogen (starch) syntha . . . 150 3e−35 gi|136758|sp|P19395|UGST_ORYSA Granule-bound glycogen [star . . . 150 3e−35 gi|7798551|gb|AAC61675.2| (AF031162) granule-bound starch s . . . 150 3e−35 gi|15451566|gb|AAK98690.1|AC069158_2 (AC069158) Putative st . . . 148 1e−34 gi|12019656|gb|AAD45815.2| (AF168786) soluble starch syntha . . . 148 1e−34 gi|5441242|dbj|BAA82346.1| (AB029546) granule-bound starch . . . 147 3e−34 gi|6318538|gb|AAF06936.1|AF110373_1 (AF110373) granule-boun . . . 146 5e−34 gi|6318540|gb|AAF06937.1|AF110374_1 (AF110374) granule-boun . . . 145 7e−34 gi|6624287|dbj|BAA88512.1| (AB029064) starch synthase (GBSS . . . 145 1e−33 gi|4760582|dbj|BAA77351.1| (AB019623) starch Synthase (GBSS . . . 145 1e−33 gi|4760584|dbj|BAA77352.1| (AB019624) starch synthase (GBSS . . . 144 2e−33 gi|15626365|emb|CAC69955.1| (AJ345045) granule-bound starch . . . 144 2e−33 gi|15597361|ref|NP_250855.1| (NC_002516) probable glycogen . . . 144 2e−33 gi|4588609|gb|AAD26156.1|AF113844_1 (AF113844) granule-boun . . . 144 2e−33 gi|7484400|pir||T07924 probable starch Synthase (EC 2.4.1.—. . . 144 3e−33 gi|6624285|dbj|BAA88511.1| (AB029063) starch synthase (GBSS . . . 144 3e−33 gi|6624281|dbj|BAA88509.1| (AB029061) starch synthase (GBSS . . . 144 3e−33 gi|17736918|gb|AAL41028.1| (AF250137) mutant granule bound . . . 144 3e−33 gi|11037536|gb|AAG27624.1|AF286320_1 (AF286320) granule bou . . . 142 6e−33 gi|136755|sp|P09842|UGST_HORVU Granule-bound glycogen [star . . . 140 2e−32 gi|18652407|gb|AAL77109.1|AF474373_6 (AF474373) granule-bou . . . 140 2e−32 gi|4760580|dbj|BAA77350.1| (AB019622) starch synthase (GBSS . . . 140 3e−32 gi|136765|sp|P27736|UGST_WHEAT Granule-bound glycogen [star . . . 139 5e−32 gi|6624283|dbj|BAA88510.1| (AB029062) starch synthase (GBSS . . . 139 7e−32 gi|228210|prf||1718316A granule-bound starch synthase [Sola . . . 138 1e−31 gi|4588607|gb|AAD26155.1|AF113843_1 (AF113843) granule-boun . . . 138 1e−31 gi|16716335|gb|AAC17969.3| (AF026420) granule-bound starch . . . 137 3e−31 gi|3493111|gb|AAD03013.1| (AF079293) granule-bound starch s . . . 135 1e−30 gi|3493079|gb|AAD02997.1| (AF079277) granule-bound starch s . . . 135 1e−30 gi|602594|emb|CAA58220.1| (X83220) starch (bacterial glycog . . . 135 1e−30 gi|12003285|gb|AAG43519.1|AF210699_1 (AF210699) granule-bou . . . 135 1e−30 gi|267196|sp|Q00775|UGST_SOLTU Granule-bound glycogen [star . . . 134 2e−30 gi|3493113|gb|AAD03014.1| (AF079294) granule-bound starch s . . . 134 2e−30 gi|3493115|gb|AAD03015.1| (AF079295) granule-bound starch s . . . 132 7e−30 gi|136757|sp|P04713|UGST_MAIZE Granule-bound glycogen [star . . . 132 9e−30 gi|3493119|gb|AAD03017.1| (AF079297) granule-bound starch s . . . 131 1e−29 gi|3493055|gb|AAD02985.1| (AF079265) granule-bound starch s . . . 131 1e−29 gi|12278481|gb|AAG48981.1| (AY010994) granule-bound starch . . . 131 1e−29 gi|3493107|gb|AAD03011.1| (AF079291) granule-bound starch s . . . 131 1e−29 gi|12278501|gb|AAG48991.1| (AY011004) granule-bound starch . . . 131 2e−29 gi|2833383|sp|Q43092|UGST_PEA Granule-bound glycogen [starc . . . 130 2e−29 gi|12278491|gb|AAG48986.1| (AY010999) granule-bound starch . . . 130 2e−29 gi|3493121|gb|AAD03018.1| (AF079298) granule-bound starch s . . . 130 4e−29 gi|12278477|gb|AAG48979.1| (AY010992) granule-bound starch . . . 129 5e−29 gi|12278479|gb|AAG48980.1| (AY010993) granule-bound starch . . . 129 6e−29 gi|12278485|gb|AAG48983.1| (AY010996) granule-bound starch . . . 129 6e−29 gi|3493057|gb|AAD02986.1| (AF079266) granule-bound starch s . . . 129 8e−29 gi|12278489|gb|AAG48985.1| (AY010998) granule-bound starch . . . 129 9e−29 gi|12278495|gb|AAG48988.1| (AY011001) granule-bound starch . . . 129 9e−29 gi|3493081|gb|AAD02998.1| (AF079278) granule-bound starch s . . . 129 9e−29 gi|3493075|gb|AAD02995.1| (AF079275) granule-bound starch s . . . 129 1e−28 gi|3493005|gb|AAD02960.1| (AF079240) granule-bound starch s . . . 128 1e−28 gi|3493085|gb|AAD03000.1| (AF079280) granule-bound starch s . . . 128 1e−28 gi|12278417|gb|AAG48949.1| (AY010962) granule-bound starch . . . 128 2e−28 gi|3493027|gb|AAD02971.1| (AF079251) granule-bound starch s . . . 128 2e−28 gi|2833381|sp|Q42857|UGST_IPOBA Granule-bound glycogen [sta . . . 127 2e−28 gi|3493077|gb|AAD02996.1| (AF079276) granule-bound starch s . . . 127 2e−28 gi|12278473|gb|AAG48977.1| (AY010990) granule-bound starch . . . 127 2e−28 gi|12278487|gb|AAG48984.1| (AY010997) granule-bound starch . . . 127 2e−28 gi|12278509|gb|AAG48995.1| (AY011008) granule-bound starch . . . 127 2e−28 gi|3493089|gb|AAD03002.1| (AF079282) granule-bound starch s . . . 127 2e−28 gi|12278514|gb|AAG48997.1| (AY011011) granule-bound starch . . . 127 2e−28 gi|3493087|gb|AAD03001.1| (AF079281) granule-bound starch s . . . 127 3e−28 gi|3493065|gb|AAD02990.1| (AF079270) granule-bound starch s . . . 127 3e−28 gi|3493093|gb|AAD03004.1| (AF079284) granule-bound starch s . . . 127 3e−28 gi|12278415|gb|AAG48948.1| (AY010961) granule-bound starch . . . 127 3e−28 gi|3493095|gb|AAD03005.1| (AF079285) granule-bound starch s . . . 127 3e−28 gi|12278463|gb|AAG48972.1| (AY010985) granule-bound starch . . . 127 3e−28 gi|3493051|gb|AAD02983.1| (AF079263) granule-bound starch s . . . 127 3e−28 gi|3493013|gb|AAD02964.1| (AF079244) granule-bound starch s . . . 127 3e−28 gi|3493099|gb|AAD03007.1| (AF079287) granule-bound starch s . . . 126 4e−28 gi|3493049|gb|AAD02982.1| (AF079262) granule-bound starch s . . . 126 4e−28 gi|3493097|gb|AAD03006.1| (AF079286) granule-bound starch s . . . 126 4e−28 gi|3493031|gb|AAD02973.1| (AF079253) granule-bound starch s . . . 126 4e−28 gi|3493007|gb|AAD02961.1| (AF079241) granule-bound starch s . . . 126 4e−28 gi|12278421|gb|AAG48951.1| (AY010964) granule-bound starch . . . 126 4e−28 gi|3493091|gb|AAD03003.1| (AF079283) granule-bound starch s . . . 126 4e−28 gi|3493059|gb|AAD02987.1| (AF079267) granule-bound starch s . . . 126 4e−28 gi|12278453|gb|AAG48967.1| (AY010980) granule-bound starch . . . 126 4e−28 gi|12278451|gb|AAG48966.1| (AY010979) granule-bound starch . . . 126 4e−28 gi|13377473|gb|AAK20725.1| (AF318769) granule-bound starch . . . 126 4e−28 gi|3493019|gb|AAD02967.1| (AF079247) granule-bound starch s . . . 126 5e−28 gi|12278443|gb|AAG48962.1| (AY010975) granule-bound starch . . . 126 6e−28 gi|12278471|gb|AAG48976.1| (AY010989) granule-bound starch . . . 125 7e−28 gi|3493067|gb|AAD02991.1| (AF079271) granule-bound starch s . . . 125 7e−28 gi|13774484|gb|AAK38881.1| (AF353519) granule-bound starch . . . 125 7e−28 gi|12278493|gb|AAG48987.1| (AY011000) granule-bound starch . . . 125 8e−28 gi|3493103|gb|AAD03009.1| (AF079289) granule-bound starch s . . . 125 8e−28 gi|12278435|gb|AAG48958.1| (AY010971) granule-bound starch . . . 125 9e−28 gi|12278423|gb|AAG48952.1| (AY010965) granule-bound starch . . . 125 1e−27 gi|13194734|gb|AAK15529.1| (AF331953) granule-bound starch . . . 125 1e−27 gi|3493071|gb|AAD02993.1| (AF079273) granule-bound starch s . . . 125 1e−27 gi|12278419|gb|AAG48950.1| (AY010963) granule-bound starch . . . 125 1e−27 gi|12278429|gb|AAG48955.1| (AY010968) granule-bound starch . . . 124 2e−27 gi|17940620|gb|AAL49697.1| (AF445158) granule-bound starch . . . 124 2e−27 gi|12278457|gb|AAG48969.1| (AY010982) granule-bound starch . . . 124 2e−27 gi|3493061|gb|AAD02988.1| (AF079268) granule-bound starch s . . . 124 2e−27 gi|3493069|gb|AAD02992.1| (AF079272) granule-bound starch s . . . 124 2e−27 gi|12278449|gb|AAG48965.1| (AY010978) granule-bound starch . . . 124 2e−27 gi|3493025|gb|AAD02970.1| (AF079250) granule-bound starch s . . . 124 2e−27 gi|12278507|gb|AAG48994.1| (AY011007) granule-bound starch . . . 124 2e−27 gi|12278511|gb|AAG48996.1| (AY011009) granule-bound starch . . . 124 2e−27 gi|3493073|gb|AAD02994.1| (AF079274) granule-bound starch s . . . 124 2e−27 gi|3493037|gb|AAD02976.1| (AF079256) granule-bound starch s . . . 124 2e−27 gi|3493117|gb|AAD03016.1| (AF079296) granule-bound starch s . . . 124 2e−27 gi|12278427|gb|AAG48954.1| (AY010967) granule-bound starch . . . 124 2e−27 gi|12278425|gb|AAG48953.1| (AY010966) granule-bound starch . . . 124 2e−27 gi|3493035|gb|AAD02975.1| (AF079255) granule-bound starch s . . . 124 2e−27 gi|12278497|gb|AAG48989.1| (AY011002) granule-bound starch . . . 124 2e−27 gi|3493021|gb|AAD02968.1| (AF079248) granule-bound starch s . . . 124 2e−27 gi|3492999|gb|AAD02957.1| (AF079237) granule-bound starch s . . . 124 3e−27 gi|3493041|gb|AAD02978.1| (AF079258) granule-bound starch s . . . 124 3e−27 gi|13774482|gb|AAK38880.1| (AF353518) granule-bound starch . . . 124 3e−27 gi|3493023|gb|AAD02969.1| (AF079249) granule-bound starch s . . . 124 3e−27 gi|12278437|gb|AAG48959.1| (AY010972) granule-bound starch . . . 123 3e−27 gi|3493083|gb|AAD02999.1| (AF079279) granule-bound starch s . . . 123 3e−27 gi|3493101|gb|AAD03008.1| (AF079288) granule-bound starch s . . . 123 4e−27 gi|12278475|gb|AAG48978.1| (AY010991) granule-bound starch . . . 123 4e−27 gi|12278469|gb|AAG48975.1| (AY010988) granule-bound starch . . . 123 4e−27 gi|13774486|gb|AAK38882.1| (AF353520) granule-bound starch . . . 123 4e−27 gi|3493015|gb|AAD02965.1| (AF079245) granule-bound starch s . . . 123 4e−27 gi|12278411|gb|AAG48946.1| (AY010959) granule-bound starch . . . 123 5e−27 gi|12278503|gb|AAG48992.1| (AY011005) granule-bound starch . . . 123 5e−27 gi|12278505|gb|AAG48993.1| (AY011006) granule-bound starch . . . 123 5e−27 gi|12278413|gb|AAG48947.1| (AY010960) granule-bound starch . . . 123 5e−27 gi|13377475|gb|AAK20726.1| (AF318770) granule-bound starch . . . 123 5e−27 gi|3493011|gb|AAD02963.1| (AF079243) granule-bound starch s . . . 122 6e−27 gi|3493001|gb|AAD02958.1| (AF079238) granule-bound starch s . . . 122 6e−27 gi|12278431|gb|AAG48956.1| (AY010969) granule-bound starch . . . 122 7e−27 gi|3493053|gb|AAD02984.1| (AF079264) granule-bound starch s . . . 122 7e−27 gi|13774480|gb|AAK38879.1| (AF353517) granule-bound starch . . . 122 7e−27 gi|17940628|gb|AAL49701.1| (AF445162) granule-bound starch . . . 122 8e−27 gi|3493047|gb|AAD02981.1| (AF079261) granule-bound starch s . . . 122 9e−27 gi|15054954|gb|AAK82785.1|AF292516_1 (AF292516) granule-bou . . . 122 9e−27 gi|3493003|gb|AAD02959.1| (AF079239) granule-bound starch s . . . 122 9e−27 gi|12278433|gb|AAG48957.1| (AY010970) granule-bound starch . . . 122 9e−27 gi|3493009|gb|AAD02962.1| (AF079242) granule-bound starch s . . . 122 1e−26 gi|15054956|gb|AAK82786.1|AF292517_1 (AF292517) granule-bou . . . 122 1e−26 gi|3493043|gb|AAD02979.1| (AF079259) granule-bound starch s . . . 122 1e−26 gi|15054922|gb|AAK82769.1|AF292500_1 (AF292500) granule-bou . . . 122 1e−26 gi|15054984|gb|AAK82800.1|AF292531_1 (AF292531) granule-bou . . . 122 1e−26 gi|17940655|gb|AAL49713.1| (AF445177) granule-bound starch . . . 122 1e−26 gi|15054990|gb|AAK82803.1|AF292534_1 (AF292534) granule-bou . . . 122 1e−26 gi|15054930|gb|AAK82773.1|AF292504_1 (AF292504) granule-bou . . . 122 1e−26 gi|15054960|gb|AAK82788.1|AF292519_1 (AF292519) granule-bou . . . 122 1e−26 gi|12278499|gb|AAG48990.1| (AY011003) granule-bound starch . . . 121 1e−26 gi|15054968|gb|AAK82792.1|AF292523_1 (AF292523) granule-bou . . . 121 1e−26 gi|3492995|gb|AAD02955.1| (AF079235) granule-bound starch s . . . 121 1e−26 gi|17432494|gb|AAL38185.1| (AY062271) granule-bound starch . . . 121 1e−26 gi|17940659|gb|AAL49715.1| (AF445179) granule-bound starch . . . 121 2e−26 gi|3493017|gb|AAD02966.1| (AF079246) granule-bound starch s . . . 121 2e−26 gi|17940626|gb|AAL49700.1| (AF445161) granule-bound starch . . . 121 2e−26 gi|17940622|gb|AAL49698.1| (AF445159) granule-bound starch . . . 121 2e−26 gi|3493033|gb|AAD02974.1| (AF079254) granule-bound starch s . . . 120 2e−26 gi|17940636|gb|AAL49705.1| (AF445166) granule-bound starch . . . 120 2e−26 gi|17940639|gb|AAL49706.1| (AF445168) granule-bound starch . . . 120 2e−26 gi|15054970|gb|AAK82793.1|AF292524_1 (AF292524) granule-bou . . . 120 3e−26 gi|3493063|gb|AAD02989.1| (AF079269) granule-bound starch s . . . 120 3e−26 gi|3493045|gb|AAD02980.1| (AF079260) granule-bound starch s . . . 120 4e−26 gi|17940634|gb|AAL49704.1| (AF445165) granule-bound starch . . . 120 4e−26 gi|3493039|gb|AAD02977.1| (AF079257) granule-bound starch s . . . 120 5e−26 gi|17940630|gb|AAL49702.1| (AF445163) granule-bound starch . . . 119 5e−26 gi|17940632|gb|AAL49703.1| (AF445164) granule-bound starch . . . 119 6e−26 gi|17940648|gb|AAL49710.1| (AF445173) granule-bound starch . . . 119 7e−26 gi|17940624|gb|AAL49699.1| (AF445160) granule-bound starch . . . 119 8e−26 gi|17940677|gb|AAL49723.1| (AF445189) granule-bound starch . . . 118 2e−25 gi|17940644|gb|AAL49708.1| (AF445171) granule-bound starch . . . 118 2e−25

[0412] Glycosyl transferase family group1 (pfam 00534)domain (“GLYTR”) of maize GBSS NKEALQAEVGLPVDRNIPLVAFIGRLEEQ Seq ID. No. 1136 KGPDVMAAAIPQLMEMVEDVQIVLLGTGKKKFERMLMSAEEKFPGKVRAVVKFNAALA HHIMAGADVLAVTSRFEPCGLIQLQGMRYGTPCACASTGGLVDTIIEGKTGFHMGRLS VDCNVVEPADVKKVATTLQRAIK Glycosyl transferase family group1 (pfam 00534)domain (“GLYTR”) of maize SSI LPIRPDVPLIGFIGRLDYQKGIDLIQLIIPDLMREDVQFVMLGSGDPELEDWMRSTESIFKDKFRGWV Seq ID. No. 1137 GFSVPVSHRITAGCDILLMPSRFEPCGLNQLYAMQYGTVPVVHATGGLRDTVENFNPF GENGEQGTGWAFAPLTTENMFVDIANCNIYIQGTQVLLGRANEARHVKRLHVGPCR Glycosyl transferase family group1 (pfam 00534)domain (GLYTR) of maize SSIIa KAALQRELGLEVRDDVPLLGFIGRLDGQKGVDIIGDAMPWIAGQDVQLVMLGTGRADLERMLQHLEREH Seq ID. No. 1138 PNKVRGWVGFSVPMAHRITAGADVLVMPSRFEPCGLNQLYAMAYGTVPVVHAVGGLRDTVAPFDPFGD AGLGWTFDRAEANKLIEALR Glycosyl transferase family group1 (pfam 00534)domain (GLYTR) of maize SSIIb QVRDDVPLIGFIGRLDHQKGVDIIADAIHWIAGQDVQLVMLGTGRADLEDMLRRFESEHSDKVRAWVGFS Seq ID. No. 1139 VPLAHRITAGADILLMPSRFEPCGLNQLYAMAYGTVPVVHAVGGLRDTVAPFDPFNDTGLGWTFDRAEA NRMID Glycosyl transferase family group1 (pfam 00534)domain (GLYTR) of maize DU1 PVV GIVTRLTAQK GIHLIKHAIHRTLERNGQVV LLGSAPDSRI QADFVNLANT LHGVNHGQVR Seq ID. No. 1140 LSLTYDEPLS HLIYAGSDFILVPSIFEPCG LTQLVAMRYG TIPIVRKTGG LFDTVFDVDN Nucleotide sequence of maize GBSS 1 CAGCGACCTA TTACACAGCC CGCTCGGGCC CGCGACGTCG GGACACATCT TCTTCCCCCT Seq ID. No. 1141 61 TTTGGTGAAG CTCTGCTCGC AGCTGTCCGG CTCCTTGGAC GTTCGTGTGG CAGATTCATC 121 TGTTGTCTCG TCTCCTGTGC TTCCTGGGTA GCTTGTGTAG TGGAGCTGAC ATGGTCTGAG 181 CAGGCTTAAA ATTTGCTCGT AGACGAGGAG TACCAGCACA GCACGTTGCG GATTTCTCTG 241 CCTGTGAAGT GCAACGTCTA GGATTGTCAC ACGCCTTGGT CGCGTCGCGT CGCGTCGCGT 301 CGATGCGGTG GTGAGCAGAG CAGCAACAGC TGGGCGGCCC AACGTTGGCT TCCGTGTCTT 361 CGTCGTACGT ACGCGCGCGC CGGGGACACG CAGCAGAGAG CGGAGAGCGAGCCGTGCACG 421 GGGAGGTGGT GTGGAAGTGG AGCCGCGCGC CCGGCCGCCC GCGCCCGGTGGGCAACCCAA 481 AAGTACCCAC GACAAGCGAA GGCGCCAAAG CGATCCAAGC TCCGGAACGC AACAGCATGC 541 GTCGCGTCGG AGAGCCAGCC ACAAGCAGCC GAGAACCGAA CCGGTGGGCG ACGCGTCATG 601 GGACGGACGC GGGCGACGCT TCCAAACGGG CCACGTACGC CGGCGTGTGC GTGCGTGCAG 661 ACGACAAGCC AAGGCGAGGC AGCCCCCGAT CGGGAAAGCG TTTTGGGCGC GAGCGCTGGC 721 GTGCGGGTCA GTCGCTGGTG CGCAGTGCCG GGGGGAACGG GTATCGTGGG GGGCGCGGGC 781 GGAGGAGAGC GTGGCGAGGG CCGAGAGCAG CGCGCGGCCG GGTCACGCAA CGCGCCCCAC 841 GTACTGCCCT CCCCCTCCGC GCGCGCTAGA AATACCGAGG CCTGGACCGG GGGGGGGCCC 901 CGTCACATCC ATCCATCGAC CGATCGATCG CCACAGCCAA CACCACCCGC CGAGGCGACG 961 CGACAGCCGC CAGGAGGAAG GAATAAACTC ACTGCCAGCC AGTGAAGGGG GAGAAGTGTA 1021 CTGCTCCGTC GACCAGTGCG CGCACCGCCC GGCAGGGCTG CTCATCTCGT CGACGACCAG 1081 GTTCTGTTCC GTTCCGATCC GATCCGATCC TGTCCTTGAG TTTCGTCCAG ATCCTGGCGC 1141 GTATCTGCGT GTTTGATGAT CCAGGTTCTT CGAACCTAAA TCTGTCCGTG CACACGTCTT 1201 TTCTCTCTCT CCTACGCAGT GGATTAATCG GCATGGCGGC TCTGGCCACG TCGCAGCTCG 1261 TCGCAACGCG CGCCGGCCTG GGCGTCCCGG ACGCGTCCAC GTTCCGCCGC GGCGCCGCGC 1321 AGGGCCTGAG GGGGGCCCGG GCGTCGGCGG CGGCGGACAC GCTCAGCATG CGGACCAGCG 1381 CGCGCGCGGC GCCCAGGCAC CAGCAGCAGG CGCGCCGCGG GGGCAGGTTC CCGTCGCTCG 1441 TCGTGTGCGC CAGCGCCGGC ATGAACGTCG TCTTCGTCGG CGCCGAGATG GCGCCGTGGA 1501 GCAAGACCGG CGGCCTCGGC GACGTCCTCG GCGGCCTGCC GCCGGCCATG GCCGTAAGCG 1561 CGCGCACCGA GACATGCATC CGTTGGATCG CGTCTTCTTC GTGCTCTTGC CGCGTGCATG 1621 ATGCATGTGT TTCCTCCTGG CTTGTGTTCG TGTATGTGAC GTGTTTGTTC GGGCATGCAT 1681 GCAGGCGAAC GGGCACCGTG TCATGGTCGT CTCTCCCCGC TACGACCAGT ACAAGGACGC 1741 CTGGGACACC AGCGTCGTGT CCGAGGTACG GCCACCGAGA CCAGATTCAG ATCACAGTCA 1801 CACACACCGT CATATGAACC TTTCTCTGCT CTGATGCCTG CAACTGCAAA TGCATGCAGA 1861 TCAAGATGGG AGACGGGTAC GAGACGGTCA GGTTCTTCCA CTGCTACAAG CGCGGAGTGG 1921 ACCGCGTGTT CGTTGACCAC CCACTGTTCC TGGAGAGGGT GAGACGAGAT CTGATCACTC 1981 GATACGCAAT TACCACCCCA TTGTAAGCAG TTACAGTGAG CTTTTTTTCC CCCCGGCCTG 2041 GTCGCTGGTT TCAGGTTTGG GGAAAGACCG AGGAGAAGAT CTACGGGCCT GTCGCTGGAA 2101 CGGACTACAG GGACAACCAG CTGCGGTTCA GCCTGCTATG CCAGGTCAGG ATGGCTTGGT 2161 ACTACAACTT CATATCATCT GTATGCAGCA GTATACACTG ATGAGAAATG CATGCTGTTC 2221 TGCAGGCAGC ACTTGAAGCT CCAAGGATCC TGAGCCTCAA CAACAACCCA TACTTCTCCG 2281 GACCATACGG TAAGAGTTGC AGTCTTCGTA TATATATCTG TTGAGCTCGA GAATCTTCAC 2341 AGGAAGCGGC CCATCAGACG GACTGTCATT TTACACTGAC TACTGCTGCT GCTCTTCGTC 2401 CATCCATACA AGGGGAGGAC GTCGTGTTCG TCTGCAACGA CTGGCACACC GGCCCTCTCT 2461 CGTGCTACCT CAAGAGCAAC TACCAGTCCC ACGGCATCTA CAGGGACGCA AAGGTTGCCT 2521 TCTCTGAACT GAACAACGCC GTTTTCGTTC TCCATGCTCG TATATACCTC GTCTGGTAGT 2581 GGTGGTGCTT CTCTGAGAAA CTAACTGAAA CTGACTGCAT GTCTGTCTGA CCATCTTCAC 2641 GTACTACCAG ACCGCTTTCT GCATCCACAA CATCTCCTAC CAGGGCCGGT TCGCCTTCTC 2701 CGACTACCCG GAGCTGAACC TCCCGGAGAG ATTCAAGTCG TCCTTCGATT TCATCGACGG 2761 GTCTGTTTTC CTGCGTGCAT GTGAACATTC ATGAATGGTA ACCCACAACT GTTCGCGTCC 2821 TGCTGGTTCA TTATCTGACC TGATTGCATT ATTGCAGCTA CGAGAAGCCC GTGGAAGGCC 2881 GGAAGATCAA CTGGATGAAG GCCGGGATCC TCGAGGCCGA CAGGGTCCTC ACCGTCAGCC 2941 CCTACTACGC CGAGGAGCTC ATCTCCGGCA TCGCCAGGGG CTGCGAGCTC GACAACATCA 3001 TGCGCCTCAC CGGCATCACC GGCATCGTCA ACGGCATGGA CGTCAGCGAG TGGGACCCCA 3061 GCAGGGACAA GTACATCGCC GTGAAGTACG ACGTGTCGAC GGTGAGCTGG CTAGCTCTGA 3121 TTCTGCTGCC TGGTCCTCCT GCTCATCATG CTGGTTCGGT ACTGACGCGG CAAGTGTACG 3181 TACGTGCGTG CGACGGTGGT GTCCGGTTCA GGCCGTGGAG GCCAAGGCGC TGAACAAGGA 3241 GGCGCTGCAG GCGGAGGTCG GGCTCCCGGT GGACCGGAAC ATCCCGCTGG TGGCGTTCAT 3301 CGGCAGGCTG GAAGAGCAGA AGGGCCCCGA CGTCATGGCG GCCGCCATCC CGCAGCTCAT 3361 GGAGATGGTG GAGGACGTGC AGATCGTTCT GCTGGTACGT GTGCGCCGGC CGCCACCCGG 3421 CTACTACATG CGTGTATCGT TCGTTCTACT GGAACATGCG TGTGAGCAAC GCGATGGATA 3481 ATGCTGCAGG GCACGGGCAA GAAGAAGTTC GAGCGCATGC TCATGAGCGC CGAGGAGAAG 3541 TTCCCAGGCA AGGTGCGCGC CGTGGTCAAG TTCAACGCGG CGCTGGCGCA CCACATCATG 3601 GCCGGCGCCG ACGTGCTCGC CGTCACCAGC CGCTTCGAGC CCTGCGGCCT CATCCAGCTG 3661 CAGGGGATGC GATACGGAAC GGTACGAGAG AAAAAAAAAA TCCTGAATCC TGACGAGAGG 3721 GACAGAGACA GATTATGAAT GCTTCATCGA TTTGAATTGA TTGATCGATG TCTCCCGCTG 3781 CGACTCTTGC AGCCCTGCGC CTGCGCGTCC ACCGGTGGAC TCGTCGACAC CATCATCGAA 3841 GGCAAGACCG GGTTCCACAT GGGCCGCCTC AGCGTCGACG TAAGCCTAGC TCTGCCATGT 3901 TCTTTCTTCT TTCTTTCTGT ATGTATGTAT GAATCAGCAC CGCCGTTCTT GTTTCGTCGT 3961 CGTCCTCTCT TCCCAGTGTA ACGTCGTGGA GCCGGCGGAC GTCAAGAAGG TGGCCACCAC 4021 ATTGCAGCGC GCCATCAAGG TGGTCGGCAC GCCGGCGTAC GAGGAGATGG TGAGGAACTG 4081 CATGATCCAG GATCTCTCCT GGAAGGTACG TACGCCCGCC CCGCCCCGCC CCGCCAGAGC 4141 AGAGCGCCAA GATCGACCGA TCGACCGACC ACACGTACGC GCCTCGCTCC TGTCGCTGAC 4201 CGTGGTTTAA TTTGCGAAAT GCGCAGGGCC CTGCCAAGAA CTGGGAGAAC GTGCTGCTCA 4261 GCCTCGGGGT CGCCGGCGGC GAGCCAGGGG TCGAAGGCGA GGAGATCGCG CCGCTCGCCA 4321 AGGAGAACGT GGCCGCGCCC TGAAGAGTTC GGCCTGCAGG GCCCCTGATC TCGCGCGTGG 4381 TGCAAAGATG TTGGGACATC TTCTTATATA TGCTGTTTCG TTTATGTGAT ATGGACAAGT 4441 ATGTGTAGCT GCTTGCTTGT GCTAGTGTAA TGTAGTGTAG TGGTGGCCAG TGGCACAACC 4501 TAATAAGCGC ATGAACTAAT TGCTTGCGTG TGTAGTTAAG TACCGATCGG TAATTTTATA 4561 TTGCGAGTAA ATAAATGGAC CTGTAGTGGT GGAGTAAATA ATCCCTGCTG TTCGGTGTTC 4621 TTATCGCTCC TCGTATAGAT ATTATATAGA GTACATTTTT CTCTCTCTGA ATCCTACGTT 4681 TGTGAAATTT CTATATCATT ACTGTAAAAT TTCTGCGTTC CAAAAGAGAC CATAGCCTAT 4741 CTTTGGCCCT GTTTGTTTCG GCTTCTGGCA GCTTCTGGCC ACCAAAAGCT GCTGCGGACT Nucleotide sequence of maize SSI 1 GAATTCGCGG CCGCCTTATT TCTGGTTGGC CACATACATC ATCCAAAAAA CTTTATTATT Seq ID. No. 1142 61 GAATTACAAC TAATAAGCAA TCTAAAAGAG GGCACCACCA ATGATGTGTT GTTGGTAGGA 121 GGCCGCTGGG TCTGTCAAAG CAAGITGGAC AAAGGGCAAC AATTGTTGTA GTTGTAAGAG 181 GGTTGCGGGG TTAGCCGCAA ACTGCTGGTA GAAAGGCAGC AACTGTTGCT GTGTCAAGAA 241 GGAAGCACGG TTTGCTGCAG CTGTTGTGCC CTGATGGTTT GTACGAATGA CTGCACCAAA 301 GATAGGGCTG GCGATTGTTG AAACAACAAG GGCGATAAAG GTATGTTGCT TGCTGCGATT 361 GCTTGTTGAA GCCTATATGG TTGAAGAGCT GGGTTTTCAC ATATTGAAGC TATAATTGAT 421 GGAAGGTATG GGGGAAGAAG GGAAGCTATA GGAGCTTGTG AGCATTGAGG GAAAATTGTC 481 GCGTTAGCAA CACATGTAGA AAGAGCAAGG AGCATAAGGA GGGAAAATAT CTTGGTCGCC 541 ATTGTTGCGC GCGATCCACG GCCCCCGCCC CCCGCGCTCC TGTCTGCTCT CCCTCTCCGC 601 AATGGCGACG CCCTCGGCCG TGGGCGCCGC GTGCCTCCTC CTCGCGCGGG CCGCCTGGCC 661 GGCCGCCGTC GGCGACCGGG CGCGCCCGCG GCGGCTCCAG CGCGTGCTGC GCCGCCGGTG 721 CGTCGCGGAG CTGAGCAGGG AGGGGCCCGC GCCGCGCCCG CTGCCACCCG CGCTGCTGGC 781 GCCCCCGCTC GTGCCCGGCT TCCTCGCGCC GCCGGCCGAG CCCACGGGTG AGCCGGCATC 841 GACGCCGCCG CCCGTGCCCG ACGCCGGCCT GGGGGACCTC GGTCTCGAAG CTGAAGGGAT 901 TGCTGAAGGT TCCATCGATA ACACAGTAGT TGTGGCAAGT GAGCAAGATT CTGAGATTGT 961 GGTTGGAAAG GAGCAAGCTC GAGCTAAAGT AACACAAAGC ATTGTCTTTG TAACCGGCGA 1021 AGCTTCTCCT TATGCAAAGT CTGGGGGTCT AGGAGATGTT TGTGGTTCAT TGCCAGTTGC 1081 TCTTGCTGCT CGTGGTCACC GTGTGATGGT TGTAATGCCC AGATATTTAA ATGGTACCTC 1041 CGATAAGAAT TATGCAAATG CATTTTACAC AGAAAAACAC ATTCGGATTC CATGCTTTGG 1201 CGGTGAACAT GAAGTTACCT TCTTCCATGA GTATAGAGAT TCAGTTGACT GGGTGTTTGT 1261 TGATCATCCC TCATATCACA GACCTGGAAA TTTATATGGA GATAAGTTTG GTGCTTTTGG 1321 TGATAATCAG TTCAGATACA CACTCCTTTG CTATGCTGCA TGTGAGGCTC CTTTGATCCT 1381 TGAATTGGGA GGATATATTT ATGGACAGAA TTGCATGTTT GTTGTCAATG ATTGGCATGC 1441 CAGTCTAGTG CCAGTCCTTC TTGCTGCAAA ATATAGACCA TATGGTGTTT ATAAAGACTC 1501 CCGCAGCATT CTTGTAATAC ATAATTTAGC ACATCAGGGT GTAGAGCCTG CAAGCACATA 1561 TCCTGACCTT GGGTTGCCAC CTGAATGGTA TGGAGCTCTG GAGTGGGTAT TCCCTGAATG 1621 GGCGAGGAGG CATGCCCTTG ACAAGGGTGA GGCAGTTAAT TTTTTGAAAG GTGCAGTTGT 1681 GACAGCAGAT CGAATCGTGA CTGTCAGTAA GGGTTATTCG TGGGAGGTCA CAACTGCTGA 1741 AGGTGGACAG GGCCTCAATG AGCTCTTAAG CTCCAGAAAG AGTGTATTAA ACGGAATTGT 1801 AAATGGAATT GACATTAATG ATTGGAACCC TGCCACAGAC AAATGTATCC CCTGTCATTA 1861 TTCTGTTGAT GACCTCTCTG GAAAGGCCAA ATGTAAAGGT GCATTGCAGA AGGAGCTGGG 1921 TTTACCTATA AGGCCTGATG TTCCTCTGAT TGGCTTTATT GGAAGGTTGG ATTATCAGAA 1981 AGGCATTGAT CTCATTCAAC TTATCATACC AGATCTCATG CGGGAAGATG TTCAATTTGT 2041 CATGCTTGGA TCTGGTGACC CAGAGCTTGA AGATTGGATG AGATCTACAG AGTCGATCTT 2101 CAAGGATAAA TTTCGTGGAT GGGTTGGATT TAGTGTTCCA GTTTCCCACC GAATAACTGC 2161 CGGCTGCGAT ATATTGTTAA TGCCATCCAG ATTCGAACCT TGTGGTCTCA ATCAGCTATA 2221 TGCTATGCAG TATGGCACAG TTCCTGTTGT CCATGCAACT GGGGGCCTTA GAGATACCGT 2281 GGAGAACTTC AACCCTTTCG GTGAGAATGG AGAGCAGGGT ACAGGGTGGG CATTCGCACC 2341 CCTAACCACA GAAAACATGT TTGTGGACAT TGCGAACTGC AATATCTACA TACAGGGAAC 2401 ACAAGTCCTC CTGGGAAGGG CTAATGAAGC GAGGCATGTC AAAAGACTTC ACGTGGGACC 2461 ATGCCGCTGA ACAATACGAA CAAATCTTCC AGTGGGCCTT CATCGGATCG ACCCGATGTT 2521 CAATGGAAAA AAGGGACCAA AGTTGGTTGG TTCCTTGAAG ATTATCAGTT CATCATCCTA 2581 TAGTAAGCTG AATGATGAAA GAAAACCCCT GTACATTACA TGGAAGGCAG ACCGGCTATT 2641 GGCTCCATTG CTCCAATGTC TGCTTTGGCT GCCTTGCCTC GATGGACCGG ATGCAGTGAG 2701 GAATCCAGNC GAACGACAGT TTTGAAGGAT AGGAAGGGGA GCTGGAAGCA GTCACGCAGG 2761 CAGGCAAGCC TTCGCCGTTA ATTCATATGG AACAAGCTGG AGTCAGTTTC TGCTGTGCCA 2821 CTCACTGTTT ACCTTAAGAT TATTACCTGT GTTGTTCTCC TTTGCTCGTT AGGGCTGATA 2881 ACATAATGAC TCATTAAGAA TATAATTCAC TCTGCCTCGT TTTTAATCTT AAGTGAAGTC 2941 GAGATCTACT TCGTCATTCC TTCCCCGTTT AAAAAAAAAA AAAAAAAAAA A Nucleotide sequence of maize SSIIa 1 GCGGCCGCTT TTTTTTAAAA TCTGTGGAGA AGGCTTTATT ATTAGCTCAT AATACTTTTG Seq ID. No. 1143 61 ATGCATCAAT AGGCCTCTCC CACCTCACAT TAGTCTCAAC ATTGACTTCA TATTATACAA 121 CCCTAAGAAG GTTGATCGGC TGCAACAATT GAAATCTAAA GACTACGTCA AGCGCTTCCC 181 TCTTGTGATA TCATCAGTTT GCTGGAACCT TGTAGCTTCC GCACTGGAAG CCATGCTCAA 241 ATGGCCTCTT ACACTGCTCA GCAACATACA CAACCTTCTC CATGCACACA ACCTTCTCAG 301 TTTCTTTGGT GACCTTGGAG CACAAGCAAG AAACGTTIGC CTTCTTGATG ACACCACAGC 361 AAGCATCCGA AGGAGGGACC TTTGGATTAG CTGGGAACAT CACGTATGTC TTGCAGTCAC 421 TTATCAGGCT TTGGAGGTCA TTCTCACAGT CTCCATCAGC ATGAGAGCCT ATGGCAAACA 481 TAGCTGCTAC AAAGGAGAGG GCTAAGAACA GGCTCAACAG TTTTGCCATG TTTACTAGTT 541 CTTGGGGGAC GCCTATTGAA AGCTGTCCGC TGCCCACCGC GTGCGCTGCG CTCCCGTGCG 601 GCACTGCCGG CGGCGCGACC CCGCGCCCAT TGGACGAGCT TCCGCCCCGC CCCGATCGAT 661 CCCGCCGCCA TGTCGTCGGC GGCCGTGTCG TCCTCTTCCT CCACCTTCTT CCTCGCGCTC 721 GCCTCCGCCT CCCCCGGGGG CCGCAGGCGG GCTAGGGTCG GCTCCTCGCC GTTCCACACC 781 GGCGCCAGCC TGAGTTTCGC GTTCTGGGCG CCACCGTCGC CGCCGCGCGC GCCCCGGGAC 841 GCAGCGCTGG TGCGCGCTGA GGCTGAGGCC GGGGGCAAGG ACGCGCCGCC GGAGAGGAGC 901 GGCGACGCCG CCAGGTTGCC CCGCGCTCGG CGCAATGCGG TCTCCAAACG GAGGGATCCT 961 CTTCAGCCGG TCGGCCGGTA CGGCTCCGCG ACGGGAAACA CGGCCAGGAC CGGCGCCGCG 1021 TCCTGCCAGA ACGCCGCATT GGCGGACGTT GAGATCAAGT CCATCGTCGC CGCGCCGCCG 1081 ACGAGCATAG TGAAGTTCCC AGCGCCGGGC TACAGGATGA TCCTTCCCTC TGGGGACATA 1041 GCGCCGGAGA CTGTCCTCCC AGCCCCGAAG CCACTGCATG AATCGCCTGC GGTTGACGGA 1201 GATTCAAATG GAATTGCACC TCCTACAGTT GAGCCATTAG TACAGGAGGC CACTTGGGAT 1261 TTCAAGAAAT ACATCGGTTT TGACGAGCCT GACGAAGCGA AGGATGATTC CAGGGTTGGT 1321 GCAGATGATG CTGGTTCTTT TGAACATTAT GGGGACAATG ATTCTGGGCC TTTGGCCGGG 1381 GAGAATGTTA TGAACGTGAT CGTGGTGGCT GCTGAATGTT CTCCATGGTG CAAAACAGGT 1441 GGTCTTGGAG ATGTTGTGGG AGCTTTACCC AAGGCTTTAG CGAGAAGAGG ACATCGTGTT 1501 ATGGTTGTGG TACCAAGGTA TGGGGACTAT GTGGAAGCCT TTGATATGGG AATCCGGAAA 1561 TACTACAAAG CTGCAGGACA GGACCTAGAA GTGAACTATT TCCATGCATT TATTGATGGA 1621 GTCGACTTTG TGTTCATTGA TGCCCCTCTT TTCCGGCACC GTCAAGATGA CATATATGGG 1681 GGAAGTAGGC AGGAAATCAT GAAGCGCATG ATTTTGTTTT GCAAGGTTGC TGTTGAGGTT 1741 CCTTGGCACG TTCCATGCGG TGGTGTGTGC TACGGAGATG GAAATTTGGT GTTCATTGCC 1801 AATGATTGGC ACACTGCACT CCTGCCTGTT TATCTGAAGG CATATTACAG AGACCATGGG 1861 TTAATGCAGT ACACTCGCTC CGTCCTCGTC ATACATAACA TCGCCCACCA GGGCCGTGGT 1921 CCTGTAGATG AATTCCCGTA CATGGACTTG CCTGAACACT ACCTTCAACA TTTCGAGCTG 1981 TACGATCCCG TCGGTGGCGA GCACGCCAAC ATCTTTGCCG CGGGTCTGAA GATGGCAGAC 2041 CGGGTGGTGA CTGTCAGCCG CGGCTACCTG TGGGAGCTGA AGACAGTGGA AGGCGGCTGG 2101 GGCCTCCACG ACATCATCCG TTCTAACGAC TGGAAGATCA ATGGCATCGT GAACGGCATC 2161 GACCACCAGG AGTGGAACCC CAAGGTGGAC GTGCACCTGC GGTCGGACGG CTACACCAAC 2221 TACTCCCTCG AGACACTCGA CGCTGGAAAG CGGCAGTGCA AGGCGGCCCT GCAGCGGGAG 2281 CTGGGCCTGG AAGTGCGCGA CGACGTGCCG CTGCTCGGCT TCATCGGGCG TCTGGATGGA 2341 CAGAAGGGCG TGGACATCAT CGGGGACGCG ATGCCGTGGA TCGCGGGGCA GGACGTGCAG 2401 CTGGTGATGC TGGGCACCGG GCGCGCCGAC CTGGAACGAA TGCTGCAGCA CTTGGAGCGG 2461 GAGCATCCCA ACAAGGTGCG CGGGTGGGTC GGGTTCTCGG TGCCTATGGC GCATCGCATC 2521 ACGGCGGGCG CCGACGTGCT GGTGATGCCT TCCCGCTTCG AGCCCTGCGG GCTGAACCAG 2581 CTCTACGCGA TGGCGTACGG CACCGTCCCT GTGGTGCACG CCGTGGGCGG GCTCAGGGAC 2641 ACCGTGGCGC CGTTCGACCC GTTCGGCGAC GCCGGGCTCG GGTGGACTTT TGACCGCGCC 2701 GAGGCCAACA AGCTGATCGA GGCGCTCAGG CACTGCCTCG ACACGTACCG GAAGTACGGG 2761 GAGAGCTGGA AGAGTCTCCA GGCGCGCGGC ATGTCGCAGG ACCTCAGCTG GGACCACGCG 2821 GCTGAGCTCT ACGAGGACGT CCTTGTCAAG GCCAAGTACC AGTGG Nucleotide sequence of maize SSIIb 1 GCGGCCGCCT GGTAGGCGCT GGTACAAGCG GAAGCAGCAG TAGCGTGAGG CATCCCCATG Seq ID. No. 1144 61 CCGGGGGCAA TCTCTTCCTC GTCGTCGGCT TTTCTCCTCC CCGTCGCGTC CTCCTCGCCG 121 CGGCGCAGGC GGGGCAGTGT GGGTGCTGCT CTGCGCTCGT ACGGCTACAG CGGCGCGGAG 181 CTGCGGTTGC ATTGGGCGCG GCGGGGCCCG CCTCAGGATG GAGCGGCGTC GGTACGCGCC 241 GCAGCGGCAC CGGCCGGGGG CGAAAGCGAG GAGGCAGCGA AGAGCTCCTC CTGGTCCCAG 301 GCGGGCGCTG TTCAGGGCAG CACGGCCAAG GCTGTGGATT CTGCTTCACC TCCCAATCCT 361 TTGACATCTG CTCCGAAGCA AAGTCAGAGC GCTGCAATGC AAAACGGAAC GAGTGGGGGC 421 AGCAGCGCGA GCACCGCCGC GCCGGTGTCC GGACCCAAAG CTGATCATCC ATCAGCTCCT 481 GTCACCAAGA GAGAAATCGA TGCCAGTGCG GTGAAGCCAG AGCCCGCAGG TGATGATGCT 541 AGACCGGTGG AAAGCATAGG CATCGCTGAA CCGGTGGATG CTAAGGCTGA TGCAGCTCCG 601 GCTACAGATG CGGCGGCGAG TGCTCCTTAT GACAGGGAGG ATAATGAACC TGGCCCTTTG 661 GCTGGGCCTA ATGTGATGAA CGTCGTCGTG GTGGCTTCTG AATGTGCTCC TTTCTGCAAG 721 ACAGGTGGCC TTGGAGATGT CGTGGGTGCT TTGCCTAAGG CTCTGGCGAG GAGAGGACAC 781 CGTGTTATGG TCGTGATACC AAGATATGGA GAGTATGCCG AAGCCCGGGA TTTAGGTGTA 841 AGGAGACGTT ACAAGGTAGC TGGACAGGAT TCAGAAGTTA CTTATTTTCA CTCTTACATT 901 GATGGAGTTG ATTTTGTATT CGTAGAAGCC CCTCCCTTCC GGCACCGGCA CAATAATATT 961 TATGGGGGAG AAAGATTGGA TATTTTGAAG CGCATGATTT TGTTCTGCAA GGCCGCTGTT 1021 GAGGTTCCAT GGTATGCTCC ATGTGGCGGT ACTGTCTATG GTGATGGCAA CTTAGTTTTC 1081 ATTGCTAATG ATTGGCATAC CGCACTTCTG CCTGTCTATC TAAAGGCCTA TTACCGGGAC 1041 AATGGTTTGA TGCAGTATGC TCGCTCTGTG CTTGTGATAC ACAACATTGC TCATCAGGGT 1201 CGTGGCCCTG TAGACGACTT CGTCAATTTT GACTTGCCTG AACACTACAT CGACCACTTC 1261 AAACTGTATG ACAACATTGG TGGGGATCAC AGCAACGTTT TTGCTGCGGG GCTGAAGACG 1321 GCAGACCGGG TGGTGACCGT TAGCAATGGC TACATGTGGG AGCTGAAGAC TTCGGAAGGC 1381 GGGTGGGGCC TCCACGACAT CATAAACCAG AACGACTGGA AGCTGCAGGG CATCGTGAAC 1441 GGCATCGACA TGAGCGAGTG GAACCCCGCT GTGGACGTGC ACCTCCACTC CGACGACTAC 1501 ACCAACTACA CGTTCGAGAC GCTGGACACC GGCAAGCGGC AGTGCAAGGC CGCCCTGCAG 1561 CGGCAGCTGG GCCTGCAGGT CCGCGACGAC GTGCCACTGA TCGGGTTCAT CGGGCGGCTG 1621 GACCACCAGA AGGGCGTGGA CATCATCGCC GACGCGATCC ACTGGATCGC GGGGCAGGAC 1681 GTGCAGCTCG TGATGCTGGG CACCGGGCGG GCCGACCTGG AGGACATGCT GCGGCGGTTC 1741 GAGTCGGAGC ACAGCGACAA GGTGCGCGCG TGGGTGGGGT TCTCGGTGCC CCTGGCGCAC 1801 CGCATCACGG CGGGCGCGGA CATCCTGCTG ATGCCGTCGC GGTTCGAGCC GTGCGGGCTG 1861 AACCAGCTCT ACGCCATGGC GTACGGGACC GTGCCCGTGG TGCACGCCGT GGGGGGGCTC 1921 CGGGACACGG TGGCGCCGTT CGACCCGTTC AACGACACCG GGCTCGGGTG GACGTTCGAC 1981 CGCGCGGAGG CGAACCGGAT GATCGACGCG CTCTCGCACT GCCTCACCAC GTACCGGAAC 2041 TACAAGGAGA GCTGGCGCGC CTGCAGGGCG CGCGGCATGG CCGAGGACCT CAGCTGGGAC 2101 CACGCCGCCG TGCTGTATGA GGACGTGCTC GTCAAGGCGA AGTACCAGTG GTGAGCGAAT 2161 TAATTGGCGA CGCGACGCCG CTCCTGTCGC AGGACCTGGA CGTTATTTAG AAGGCTCTTC 2221 TCCCTGGCGG CTTTGATGCG TGCGTCGCAT TTGCGCCGGG CGGACGGGCG ACGGTGGTTG 2281 GCCTACCGCC TACGTCGGCT GCGTGCCCTG GGAATTTGGG CGGGCACGAT GATGCCACTG 2341 GGCACCGGGC GCGGGGTAGT ATGATATGAA ACCGACGGCG ATGGAGATGA GGCGCATGGC 2401 ATTTTCCCAC TGATAAATGG GGAGTTGTAT GCTACTTTAA TATCGCCACT CCTGTTAGTA 2461 TTTATATTGA TGGCGGCCGC Nucleotide sequence of maize Du1 1 GAATTCCCTA GTTCAGAGAA AGAAAGAAGT TGAGAATGAG AAGCAAGTGA GGCGCGTTTG Seq ID. No. 1145 61 CTGGGAAGTG GTTCTTGTGA GGTTTAGGAG TTCACCCTTT TTTTCTTCCC CTTCTAGAAA 121 TGGAGATGGT CCTACGGTCG CAGAGCCCTC TCTGCCTTCG GAGTGGGCCG GTGCTCATTT 181 TTCGACCAAC CGTCGCGGGC GGAGGAGGOG GCACTCAGTC TTTGTTGAGG ACTACCAGAT 241 TTGCGAGAAG AAGGGTCATT CGATGCGTTG TAGCAAGTCC AGGTTGTCCT AATAGGAAAT 301 CTAGGACAGC GTCTCCCAAC GTAAAAGTAG CTGCTTATAG CAACTATGCG CCAAGACTCC 361 TCGTTGAGTC AAGCTCCAAG AAGAGCGAAC ACCATGATAG CAGCAGACAC CGTGAAGAAA 421 CTATTGATAC ATACAATGQG CTGTCAGGTT CTGATGCAGC AGAATTGACA AGTAATAGAG 481 ATGTAGAAAT TGAAGTGGAT TTGCAGCACA TTTCTGAGGA GGAATTGCCA GGAAAAGTAT 541 CGATTAATGC ATCATTAGGA GAAATGGAAA CAGTGGATGA AGCTGAGGTC GAGGAGGATA 601 AGTTTGAGGT AGATACCTCA GGAATTGTAT TGCGCAATGT TGCAGTTCGG GAAGTGGATC 661 CAAAGGATGA ACATAATGCT AAAGATGTAT TTGTGGTAGA TTCGTCAGGA ACTGCACCAG 721 ATAATGCTGC AGTGGAGGAA GTGGTAGATG AAGCTGAGGT TGAAGAGGAT ATGGTTGATG 781 TGGATATCTT GGGACTTGAC TTGAATAATG CAACGATCGA GGAAATTGAT TTGATGGAAG 841 AGGCTTTACT GGAGAACTTC GACGTGGATT CACCAGGCAA TGCTTCTAGT GGTCGAACCT 901 ATGGGGGTGT GGATGAGTTG GGTGAGCTGC CTTCAACATC CGTGGATTGC ATCGCCATTA 961 ACGGAAAACG TAGAAGTTTG AAGCCTAAGC CCTTGCCAAT TGTCAGGTTC CAGGAACAAG 1021 AACAGATAGT TTTAAGCATT GTTGACGAAG AAGGGTTGAT TGCTAGTTCA TGTGAAGAAG 1081 GCCAACCGGT GGTAGATTAC GATAAGCAAG AGGAAAACTC TACCGCTTTC GATGAACAGA 1041 AGCAATTAAC TGATGATTTC CCTGAAGAAG GCATATCTAT AGTTCACTTC CCTGAGCCAA 1201 ACAATGATAT TGTTGGATCC TCAAAATTCT TGGAGCAAAA ACAAGAATTG GATGGTTCTT 1261 ATAAACAAGA TCGATCAACC ACTGGATTGC ATGAACAAGA TCAGTCTGTT GTTAGTTCAC 1321 ACGGACAAGA TAAATCAATT GTTGGTGTGC CTCAGCAAAT CCAGTACAAT GATCAATCTA 1381 TTGCTGGTTC TCATAGACAA GATCAATCAA TTGCCGGTGC ACCTGAGCAA ATCCAATCCG 1441 TTGCTGGCTA TATAAAACCA AATCAATCTA TTGTTGGTTC TTGTAAACAA CATGAATTGA 1501 TTATTCCTGA GCCTAAGAAA ATCGAATCCA TCATCAGTTA CAATGAAATA GATCAATCTA 1561 TTGTTGGTTC TCACAAACAA GACAAATCTG TTGTTAGTGT GCCTGAGCAA ATCCAATCCA 1621 TTGTTAGTCA CAGCAAACCA AATCAATCTA CTGTTGATTC TTATAGACAA GCTGAATCAA 1681 TTATTGGTGT GCCTGAGAAA GTCCAATCCA TCACCAGTTA CGATAAACTA GACCAGTCCA 1741 TTGTTGGTTC TCTTAAACAA GATGAGCCTA TTATTAGCGT GCCTGAGAAA ATCCAATCCA 1801 TTGTCCATTA CACTAAACCA AATCAGTCTA TTGTTGGCTT GCCCAAACAA CAACAATCAA 1861 TTGTTCATAT CGTTGAACCA AAACAGTCCA TAGATGGTTT CCCTAAACAA GATCTATCAA 1921 TCGTTGGTAT CTCCAATGAG TTTCAAACAA AGCAACTGGC TACTGTTGGG ACTCATGATG 1981 GATTGCTTAT GAAGGGTGTG GAAGCTAAGG AGACATCTCA AAAGACTGAA GGGGATACAC 2041 TTCAGGCAAC GTTCAATGTC GACAACTTGT CACAGAAACA GGAAGGCTTA ACTAAAGAAG 2101 CAGACGAGAT AACAATTATT GAGAAAATCA ATGATGAAGA CCTTGTGATG ATTGAAGAAC 2161 AGAAAAGCAT AGCCATGAAT GAAGAACAGA CGATTGTTAC CGAAGAAGAC ATTCCAATGG 2221 CTAAGGTTGA GATAGGAATT GACAAGGCCA AATTTTTACA TCTGCTTTCT GAAGAAGAGA 2281 GTTCATGGGA TGAAAATGAA GTGGGAATAA TTGAGGCTGA TGAACAGTAT GAAGTCGATG 2341 AGACATCTAT GTCCACTGAA CAAGATATCC AGGAATCACC TAATGATGAT TTGGATCCAC 2401 AAGCACTATG GAGTATGCTT CAAGAGCTTG CTGAAAAAAA TTATTCGCTG GGAAACAAGT 2461 TGTTTACTTA TCCAGATGTA TTGAAAGCTG ATTCAACAAT TGATCTCTAT TTCAATCGTG 2521 ATCTATCAGC TGTGGCCAAT GAGCCTGATG TACTTATCAA AGGAGCATTC AATGGGTGGA 2581 AGTGGAGATT TTTCACTGAA AAATTGCACA AGAGCGAGCT GGCAGGGGAC TGGTGGTGCT 2641 GCAAACTATA CATTCCTAAG CAGGCATACA GAATGGACTT TGTGTTTTTT AACGGACACA 2701 CGGTATATGA AAATAATAAC AATAATGATT TCGTGATACA AATAGAAAGC ACCATGGATG 2761 AAAATTTATT TGAGGATTTC TTGGCTGAAG AAAAGCAACG AGAACTTGAG AACCTTGCAA 2821 ATGAGGAAGC TGAAAGGAGG AGACAAACTG ATGAGCAGCG GCGAATGGAG GAAGAAAGGG 2881 CCGCAGATAA AGCTGACAGG GTACAAGCCA AGGTTGAGGT AGAGACGAAG AAGAATAAAT 2941 TGTGCAATGT ATTGGGTTTA GCCAGAGCTC CTGTTGATAA TTTATGGTAC ATTGAGCCCA 3001 TCACGACTGG ACAAGAGGCT ACTGTCAGAT TGTATTATAA CATAAACTCA AGACCTCTAG 3061 TTCACAGTAC TGAGATATGG ATGCATGGTG GCTATAACAA TTGGATTGAT GGACTCTCTT 3121 TTGCTGAAAG GCTTGTTCAT CATCATGACA AAGATTGTGA TTGGTGGTTT GCAGATGTTG 3181 TCGTGCCTGA AAGAACATAT GTATTGGACT GGGTTTTTGC TGACGGCCCA CCAGGGAGTG 3241 CAAGGAATTA TGACAACAAT GGAGGACATG ATTTTCATGC TACCCTTCCA AATAACATGA 3301 CTGAGGAAGA GTATTGGATG GAAGAAGAAC AAAGGATCTA TACAAGGCTT CAACAAGAGA 3361 GGAGGGAAAG GGAGGAGGCT ATTAAAAGGA AGGCTGAGAG AAATGCAAAA ATGAAAGCTG 3421 AGATGAAGGA AAAGACTATG AGAATGTTCC TGGTTTCTCA GAAACACATT GTTTACACCG 3481 AACCACTTGA AATACATGCT GGAACTACTA TTGATGTGCT TTATAATCCT TCTAATACAG 3541 TTCTAACTGG AAAGCCAGAG GTTTGGTTTC GATGTTCCTT TAATCGTTGG ATGTATCCAG 3601 GTGGGGTGTT GCCACCTCAG AAGATGGTAC AAGCAGAAAA TGGTTCACAC CTAAAAGCAA 3661 CAGTTTACGT TCCACGAGAT GCCTATATGA TGGACTTCGT TTTCTCGGAG TCAGAAGAAG 3721 GTGGAATTTA TGATAACAGA AATGGGTTAG ACTATCATAT TCCTGTTTTT GGGTCAATTG 3781 CAAAGGAACC ACCTATGCAC ATTGTCCACA TTGCTGTTGA GATGGCACCA ATCGCAAAGG 3841 TTGGAGGTCT TGGTGATGTT GTCACTAGTC TTTCACGTGC TGTGCAAGAT TTAGGACACA 3901 ATGTGGAGGT TATTCTTCCA AAGTACGGTT GCTTGAATCT AAGCAATGTC AAGAATCTAC 3961 AAATCCATCA GAGTTTTTCT TGGGGTGGTT CTGAAATAAA TGTGTGGCGT GGACTAGTCG 4021 AAGGCCTTTG TGTTTACTTC CTGGAACCTC AAAATGGGAT GTTTGGAGTC GGATATGTAT 4081 ATGGCAGGGA CGATGACCGC CGATTTGGCT TCTTCTGTCG TTCTGCTCTA GAGTTTCTCC 4141 TCCAAAGTGG ATCTTCTCCG AACATAATAC ATTGCCATGA TTGGTCAAGT GCTCCTGTTG 4201 CCTGGCTACA CAAGGAAAAC TACGCGAAGT CTAGCTTGGC AAACGCACGG GTGGTATTCA 4261 CCATCCACAA TCTTGAATTT GGAGCGCATC ATATTGGCAA AGCAATGAGA TATTGTGATA 4321 AAGCAACAAC TGTCTCTAAT ACATATTCAA AGGAAGTGTC AGGTCATGGT GCCATAGTTC 4381 CTCATCTTGG GAAATTCTAT GGCATTCTCA ATGGAATTGA TCCGGATATA TGGGATCCGT 4441 ACAATGACAA CTTTATCCCG GTCCACTACA CTTGTGAGAA TGTGGTTGAA GGCAAGAGGG 4501 CTGCTAAGAG GGCACTGCAG CAGAAGTTTG GGTTACAGCA AATCGATGTC CCCGTCGTAG 4561 GAATCGTCAC TCGCCTGACA GCCCAAAAGG GGATCCACCT GATCAAGCAT GCGATTCACC 4621 GTACACTCGA ACGGAACGGA CAGGTGGTTT TGCTTGGTTC AGCGCCGGAC TCTCGAATCC 4681 AAGCTGATTT TGTCAACCTG GCGAATACGC TCCACGGCGT AAACCATGGG CAAGTGAGGC 4741 TTTCCTTGAC CTACGACGAG CCTCTCTCGC ATCTGATATA CGCTGGCTCT GACTTCATTC 4801 TGGTCCCATC TATATTTGAG CCTTGCGGCC TAACTCAGCT CGTCGCCATG CGGTATGGAA 4861 CCATCCCGAT TGTCCGCAAG ACTGGAGGGC TCTTCGACAC TGTCTTCGAT GTGGACAATG 4921 ACAAGGAACG AGCCCGAGAT CGAGGCCTTG AGCCCAACGG GTTTAGCTTT GACGGAGCTG 4981 ATAGCAACGG TGTTGACTAC GCGCTGAACA GGGCGATCTC AGCTTGGTTC GATGCCCGGA 5041 GCTGGTTCCA CTCCCTTTGC AAGAGAGTCA TGGAGGAGGA CTGGTCGTGG AACCGACCTG 5101 CCCTCGACTA CATCGAGCTC TACCGTTCAG CGTCCAAATT GTAATAATCC AAACAACGGC 5161 CAATGTAGTG TGTTGTCTGC AGGTCTCAGA TGCAGCCATT CAGCTTTTGC AGGTTCCTGG 5221 GCATTGCTGT ACAGCCTCCT TGTCTTTAGT TAGCTCCATT CCCCGAGGAG CACAGTGCAA 5281 TTTTTTATCC TCAGTTATTA TGCATAGATT GTCTCAGTAG AATGCTTTCT TCGGGCATGT 5341 ATGTTTGTTT CCTCTGTTGT TGAATTCTGG TGTTAAGTCG CGTATAGGAA TCTACAGGAA 5401 ATGAAAAAGT CCATTTCCTG CGTCAACCTT TTAGGGCTAC CATGCACATG AGACCTTTCA 5461 AGTGCAAAGA ATATTAGGAC TAGACTACTA GTATGTGAAC TCTATTTTTC CAAGAGATTT 5521 CAATTTTTCC AATGAAAAAT AAACTAATTT TTCTTGGAAA AATGGAAATC CCTTGGAAAA 5581 ATGGGGTTCC CAAACTAGCC CGTAGAGTAT AGATCATAGA ATTGGTCTAG TGGTTCCTCG 5641 AGAGAGAAAA AAACATAGAC TTTTCTTGTC ATATGCTTAT TTAAGTTTAT TTTGTACAAA 5701 CTTTGAGAAC CTTCAAAAAC ACCCCAATGG CTGGTTAAGT GACCAGGGAA ATAAAGAGGA 5761 TCTATAGGGA GGAATCCCCC GCCTCTCTCT CACAGATGTT GCCTAGCACC GGCCAGCCTC 5821 ATCCGTCCAG TGGAATTAAG GTTGGTTGCG ACGACAGCCC ATCAATGGAA ACCAACCTCG 5881 TGCCCCGTGC CGGGATCTAC CTTCCTTCCT CACCACCACG CCGATCTCAC CTTCCATAGG 5941 AGCTTCCTAT GCACTGTTAC CTATTATAGG TACATGACAT TGTACATCTT TGTATGAACT 6001 TACATCAATG CCAAAAATCC GGAATTC C-terminal end (“CTEND”) of maize GBSS; K V V G T P A Y E E M V R N C M I Q D L S W K G P A K N W E N V L L S L G V A Seq ID. No. 1146 G G E P G V E G E E I A P L A K E N V A A P C-terminal end (“CTEND”) of maize SSI; G E Q G T G W A F A P L T T E N M F V D I A N C N I Y I Q G T Seq ID. No. 1147 Q V L L G R A N E A R H V K R L H V G P C R C-terminal end (“CTEND”) of maize SSIIa; H C L D T Y R K Y G E S W K S L Q A R G M S Q D L S W D H A A E L Seq ID. No. 1148 Y E D V L V K A K Y Q W C-terminal end (“CTEND”) of maize SSIIb; N R M I D A L S H C L T T Y R N Y K E S W R A C R A R G M A E D L S W D H A A Seq ID. No. 1149 V L Y E D V L V K A K Y Q W C-terminal end (“CTEND”) of maize SSIII (Du-1); N D K E R A R D R G L E P N G F S F D G A D S N G V D Y A L N R A I S A W F D Seq ID. No. 1150 A R S W F H S L C K R V M E Q D W S W N R P A L D Y I E L Y R S A S K L

[0413] TABLE XXXVII List of Glucan Transferases with Different Database Accession Identifications 1: NP_385953 1. PHOSPHOGLYCEROL TRANSFERASE, CYCLIC BETA-1,2-GLUCAN MODIFICATION PROTEIN [Sinorhizobium meliloti] gi|15965600|ref|NP_385953.1|[15965600] 2: Q9SD76 Alpha-glucan phosphorylase, H isozyme (Starch phosphorylase H) gi|14916634|sp|Q9SD76|PHSH_ARATH[14916634] 3: Q9LKJ3 Alpha-glucan phosphorylase, H isozyme (Starch phosphorylase H) gi|14916632|sp|Q9LKJ3|PHSH_WHEAT[14916632] 4: Q9PKU9 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|14194917|sp|Q9PKU9|MALQ_CHLMU[14194917] 5: Q9Z1E4 Glycogen [starch] synthase, muscle gi|12230199|sp|Q9Z1E4|GYS1_MOUSE[12230199] 6: Q9VFC8 Putative glycogen [starch] synthase gi|12230129|sp|Q9VFC8|GYS_DROME[12230129] 7: Q9U2D9 Putative glycogen [starch] synthase gi|12230128|sp|Q9U2D9|GYS_CAEEL[12230128] 8: Q9Y704 Cell wall alpha-1,3-glucan synthase mok14 gi|11386958|sp|Q9Y704|MOKE_SCHPO[11386958] 9: P27472 Glycogen [starch] synthase, isoform 2 gi|1717973|sp|P27472|GYS2_YEAST[1717973] 10: P54840 Glycogen [starch] synthase, liver gi|1717972|sp|P54840|GYS2_HUMAN[1717972] 11: P54859 Glycogen [starch] synthase, brain gi|1717968|sp|P54859|GYS3_MOUSE[1717968] 12: P13807 Glycogen [starch] synthase, muscle gi|1351366|sp|P13807|GYS1_HUMAN[1351366] 13: P17625 Glycogen [starch] synthase, liver gi|136764|sp|P17625|GYS2_RAT[136764] 14: P23337 Glycogen [starch] synthase, isoform 1 gi|136753|sp|P23337|GYS1_YEAST[136753] 15: P04045 Alpha-1,4 glucan phosphorylase, L-1 isozyme, chloroplast precursor (Starch phosphorylase L-1) gi|130173|sp|P04045|PHS1_SOLTU[130173] 16: P27598 Alpha-1,4 glucan phosphorylase, L isozyme, chloroplast precursor (Starch phosphorylase L) gi|130172|sp|P27598|PHSL_IPOBA[130172] 17: O93869 Glycogen [starch] synthase gi|12230121|sp|O93869|GYS_NEUCR[12230121] 18: P80099 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6226644|sp|P80099|MGTA_THEMA[6226644] 19: O87172 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6225654|sp|O87172|MALQ_THEAQ[6225654] 20: P72785 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6225653|sp|P72785|MALQ_SYNY3[6225653] 21: O53932 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6225652|sp|O53932|MALQ_MYCTU[6225652] 22: O84089 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6225650|sp|O84089|MALQ_CHLTR[6225650] 23: O66937 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|6225647|sp|O66937|MALQ_AQUAE[6225647] 24: P13031 Glycogen phosphorylase gi|2851413|sp|P13031|PHSG_ECOLI[2851413] 25: P53536 Alpha-1,4 glucan phosphorylase, L isozyme, chloroplast precursor (Starch phosphorylase L) gi|2506470|sp|P53536|PHSL_VICFA[2506470] 26: P53535 Alpha-1,4 glucan phosphorylase, L-2 isozyme, chloroplast precursor (Starch phosphorylase L-2) gi|1730557|sp|P53535|PHS2_SOLTU[1730557] 27: P52981 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) gi|1707936|sp|P52981|GLGB_SYNY3[1707936] 28: Q10625 Probable 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) gi|1707934|sp|Q10625|GLGB_MYCTU[1707934] 29: P45176 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|1170869|sp|P45176|MALQ_HAEIN[1170869] 30: P15977 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|1170868|sp|P15977|MALQ_ECOLI[1170868] 31: P30924 1,4-alpha-glucan branching enzyme (Starch branching enzyme) (Q-enzyme) gi|1169912|sp|P30924|GLGB_SOLTU[1169912] 32: P45177 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) gi|1169910|sp|P45177|GLGB_HAEIN[1169910] 33: P38678 Glucan synthase-1 (1,3-beta-glucan synthase) (UDP-glucose-1,3-beta-D-glucan glucosyltransferase) gi|729636|sp|P38678|GS1_NEUCR[729636] 34: P39118 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) gi|729579|sp|P39118|GLGB_BACSU[729579] 35: Q04446 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) (Brancher enzyme) gi|544388|sp|Q04446|GLGB_HUMAN[544388] 36: Q06801 4-alpha-glucanotransferase, chloroplast precursor (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|544184|sp|Q06801|DPEP_SOLTU[544184] 37: Q06119 Diacylglycerol kinase (DAGK) (Diglyceride kinase) (DGK) gi|462437|sp|Q06119|KDGL_RHIME[462437] 38: P32434 Type I protein geranylgeranyltransferase beta subunit (Type I protein geranyl-geranyltransferase beta subunit) (GGTase-I-beta) (PGGT) gi|416853|sp|P32434|CWG2_SCHPO[416853] 39: P29851 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|266497|sp|P29851|MALQ_STRPN[266497] 40: P07762 1,4-alpha-glucan branching enzyme (Glycogen branching enzyme) gi|121296|sp|P07762|GLGB_ECOLI[121296] 41: O32462 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|18202015|sp|O32462|MALQ_THELI[18202015] 42: O32450 4-alpha-glucanotransferase (Amylomaltase) (Disproportionating enzyme) (D-enzyme) gi|18202014|sp|O32450|MALQ_PYRKO[18202014] 43: Q08047 1,4-alpha-glucan branching enzyme IIB, chloroplast precursor (Starch branching enzyme IIB) (Q-enzyme) gi|1169911|sp|Q08047|GLGB_MAIZE[1169911] 44: Q9Z6V8 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17367290|sp|Q9Z6V8|GLGA_CHLPN[17367290] 45: Q9WZZ7 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17367208|sp|Q9WZZ7|GLGA_THEMA[17367208] 46: Q9RWS1 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17367076|sp|Q9RWS1|GLGA_DEIRA[17367076] 47: Q9RNH6 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17367070|sp|Q9RNH6|GLGA_RHOSH[17367070] 48: Q9PLC3 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17367025|sp|Q9PLC3|GLGA_CHLMU[17367025] 49: Q9KRB6 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366937|sp|Q9KRB6|GLGA_VIBCH[17366937] 50: Q9KDX6 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366934|sp|Q9KDX6|GLGA_BACHD[17366934] 51: Q9I1V0 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366864|sp|Q9I1V0|GLGA_PSEAE[17366864] 52: Q9EUT5 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366749|sp|Q9EUT5|GLGA_RHITR[17366749] 53: Q9CN91 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366721|sp|Q9CN91|GLGA_PASMU[17366721] 54: Q9CHM9 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366711|sp|Q9CHM9|GLGA_LACLA[17366711] 55: Q985P2 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366611|sp|Q985P2|GLGA_RHILO[17366611] 56: Q97QS5 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366608|sp|Q97QS5|GLGA_STRPN[17366608] 57: Q97GX6 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366595|sp|Q97GX6|GLGA_CLOAB[17366595] 58: P72623 Probable glycogen synthase 2 (Starch [bacterial glycogen] synthase 2) gi|17366372|sp|P72623|GLG2_SYNY3[17366372] 59: P58395 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366350|sp|P58395|GLGA_THECA[17366350] 60: P58394 Glycogen synthase 2 (Starch [bacterial glycogen] synthase 2) gi|17366347|sp|P58394|GLG2_RHIME[17366347] 61: P58393 Glycogen synthase 1 (Starch [bacterial glycogen] synthase 1) gi|17366344|sp|P58393|GLG1_RHIME[17366344] 62: O84804 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366221|sp|O84804|GLGA_CHLTR[17366221] 63: O66935 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|17366197|sp|O66935|GLGA_AQUAE[17366197] 64: P35573 Glycogen debranching enzyme (Glycogen debrancher) [Includes: 4-alpha-glucanotransferase (Oligo-1,4-1,4-glucantransferase); Amylo-alpha-1,6- glucosidase (Amylo-1,6-glucosidase) (Dextrin 6-alpha-D-glucosidase)] gi|8928542|sp|P35573|GDE_HUMAN[8928542] 65: Q59001 Probable glycogen synthase (Starch [bacterial glycogen] synthase) gi|2842612|sp|Q59001|GLGA_METJA[2842612] 66: P74521 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|2829618|sp|P74521|GLGA_SYNY3[2829618] 67: O08328 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|2811062|sp|O08328|GLGA_BACST[2811062] 68: P45179 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|1169909|sp|P45179|GLGA_HAEIN[1169909] 69: P08323 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|1169908|sp|P08323|GLGA_ECOLI[1169908] 70: P39125 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|729578|sp|P39125|GLGA_BACSU[729578] 71: P39670 Glycogen synthase (Starch [bacterial glycogen] synthase) gi|729577|sp|P39670|GLGA_AGRTU[729577] 72: P35574 Glycogen debranching enzyme (Glycogen debrancher) [Includes: 4-alpha-glucanotransferase (Oligo-1,4-1,4-glucantransferase); Amylo-alpha-1,6- glucosidase (Amylo-1,6-glucosidase) (Dextrin 6-alpha-D-glucosidase)] gi|544379|sp|P35574|GDE_RABIT[544379] 73: P05416 Glycogen synthase (Starch [bacterial glycogen] synthase) (Fragment) gi|121295|sp|P05416|GLGA_SALTY[121295] 74: 1G5AA Chain A, Amylosucrase From Neisseria Polysaccharea gi|16974797|pdb|1G5A|A[16974797] 75: B26206 alpha-1,4-glucan-protein synthase (UDP-forming) (EC 2.4.1.112) - rabbit (fragment) gi|89923|pir||B26206[89923] 76: P30538 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|232168|sp|P30538|GLGB_BACST[232168] 77: Q9UUL4 CELL WALL ALPHA-1,3-GLUCAN SYNTHASE MOK12 gi|11386953|sp|Q9UUL4|MOKC_SCHPO[11386953] 78: CAC46426 PHOSPHOGLYCEROL TRANSFERASE, CYCLIC BETA-1,2-GLUCAN MODIFICATION PROTEIN [Sinorhizobium meliloti] gi|15074781|emb|CAC46426.1|[15074781] 79: Q09854 CELL WALL ALPHA-1,3-GLUCAN SYNTHASE MOK11 gi|12644399|sp|Q09854|MOKB_SCHPO[12644399] 80: P13834 GLYCOGEN [STARCH] SYNTHASE, MUSCLE gi|12644124|sp|P13834|GYS1_RABIT[12644124] 81: P10249 SUCROSE PHOSPHORYLASE (SUCROSE GLUCOSYLTRANSFERASE) (GLUCOSYLTRANSFERASE-A) (GTF-A) gi|121726|sp|P10249|SUCP_STRMU[121726] 82: Q9Y719 CELL WALL ALPHA-1,3-GLUCAN SYNTHASE MOK13 gi|12643961|sp|Q9Y719|MOKD_SCHPO[12643961] 83: Q9USK8 CELL WALL ALPHA-1,3-GLUCAN SYNTHASE MOK1 gi|12643908|sp|Q9USK8|MOK1_SCHPO[12643908] 84: Q9Z8L2 4-ALPHA-GLUCANOTRANSFERASE (AMYLOMALTASE) (DISPROPORTIONATING ENZYME) (D-ENZYME) gi|6225648|sp|Q9Z8L2|MALQ_CHLPN[6225648] 85: S41686 geranylgeranyltransferase type I (EC 2.5.1.-) beta chain - fission yeast (Schizosaccharomyces pombe) gi|542213|pir||S41686[542213] 86: O86956 4-ALPHA-GLUCANOTRANSFERASE (AMYLOMALTASE) (DISPROPORTIONATING ENZYME) (D-ENZYME) gi|6225664|sp|O86956|MGTA_THENE[6225664] 87: Q59266 4-ALPHA-GLUCANOTRANSFERASE (AMYLOMALTASE) (DISPROPORTIONATING ENZYME) (D-ENZYME) gi|6225651|sp|Q59266|MALQ_CLOBU[6225651] 88: O34022 4-ALPHA-GLUCANOTRANSFERASE (AMYLOMALTASE) (DISPROPORTIONATING ENZYME) (D-ENZYME) gi|6225649|sp|O34022|MALQ_CHLPS[6225649] 89: AAD37783 glucan synthase [Paracoccidioides brasiliensis] gi|5007025|gb|AAD37783.1|AF148715_1[5007025] 90: NQECA 1,4-alpha-glucan branching enzyme (EC 2.4.1.18) - Escherichia coli gi|66573|pir||NQECA[66573] 91: P49331 GLUCOSYLTRANSFERASE-S PRECURSOR (GTF-S) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|6166192|sp|P49331|GTFD_STRMU[6166192] 92: P08987 GLUCOSYLTRANSFERASE-I PRECURSOR (GTF-I) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|6166191|sp|P08987|GTFB_STRMU[6166191] 93: P13470 GLUCOSYLTRANSFERASE-SI PRECURSOR (GTF-SI) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|121728|sp|P13470|GTFC_STRMU[121728] 94: P53537 ALPHA-GLUCAN PHOSPHORYLASE, H ISOZYME (STARCH PHOSPHORYLASE H) gi|1730560|sp|P53537|PHSH_VICFA[1730560] 95: P32811 ALPHA-GLUCAN PHOSPHORYLASE, H ISOZYME (STARCH PHOSPHORYLASE H) gi|417488|sp|P32811|PHSH_SOLTU[417488] 96: P52979 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|3915711|sp|P52979|GLGB_AGRTU[3915711] 97: Q04952 PUTATIVE 1,3-BETA-GLUCAN SYNTHASE COMPONENT (1,3-BETA-D-GLUCAN-UDP GLUCOSYLTRANSFERASE) gi|2498415|sp|Q04952|GLS3_YEAST[2498415] 98: P40989 1,3-BETA-GLUCAN SYNTHASE COMPONENT GLS2 (1,3-BETA-D-GLUCAN-UDP GLUCOSYLTRANSFERASE) gi|1707982|sp|P40989|GLS2_YEAST[1707982] 99: P52980 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|1707935|sp|P52980|GLGB_STRAU[1707935] 100: P38631 1,3-BETA-GLUCAN SYNTHASE COMPONENT GLS1 (1,3-BETA-D-GLUCAN-UDP GLUCOSYLTRANSFERASE) (CND1 PROTEIN) (CWN53 PROTEIN) (FKS1 PROTEIN) (PAPULACANDIN B SENSITIVITY PROTEIN 1) gi|1346146|sp|P38631|GLS1_YEAST[1346146] 101: P32775 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|729580|sp|P32775|GLGB_YEAST[729580] 102: Q01401 1,4-ALPHA-GLUCAN BRANCHING ENZYME (STARCH BRANCHING ENZYME) (Q-ENZYME) gi|399544|sp|Q01401|GLGB_ORYSA[399544] 103: P30539 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|232169|sp|P30539|GLGB_BUTFI[232169] 104: P30537 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|232167|sp|P30537|GLGB_BACCL[232167] 105: P29336 GLUCOSYLTRANSFERASE-S PRECURSOR (GTF-S) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|121729|sp|P29336|GTFS_STRDO[121729] 106: P27470 GLUCOSYLTRANSFERASE-I PRECURSOR (GTF-I) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|121725|sp|P27470|GTF2_STRDO[121725] 107: P11001 GLUCOSYLTRANSFERASE-I PRECURSOR (GTF-I) (DEXTRANSUCRASE) (SUCROSE 6-GLUCOSYLTRANSFERASE) gi|121724|sp|P11001|GTF1_STRDO[121724] 108: P16954 1,4-ALPHA-GLUCAN BRANCHING ENZYME (GLYCOGEN BRANCHING ENZYME) gi|121297|sp|P16954|GLGB_SYNP7[121297] 109: AAB41531 cyclic beta-1,2-glucan modification protein; phosphoglycerol transferase [Sinorhizobium meliloti] gi|4733934|gb|AAB41531.2|[4733934] 110: AAC62210 beta-(1-3)-glucosyl transferase [Bradyrhizobium japonicum] gi|3687658|gb|AAC62210.1|[3687658] 111: AAC61753 beta-1,3 glucan transferase Bg|2p [Pichia jadinii] gi|3661545|gb|AAC61753.1|[3661545] 112: AAB46846 alpha-1,4-glucan orthophosphate glycosyl transferase; myophosphorylase; glycogen phosphorylase isozyme [Bos taurus] gi|1836054|gb|AAB46846.1|[1836054] 113: AAB03100 starch branching enzyme class II [Arabidopsis thaliana] gi|726490|gb|AAB03100.1|[726490] 114: AAB03099 starch branching enzyme class II [Arabidopsis thaliana] gi|619939|gb|AAB03099.1|[619939] 115: CAA78143 dimethylallyltransferase [Schizosaccharomyces pombe] gi|396477|emb|CAA78143.1|[396477] 116: AAA34632 1,4-glucan-6-(1,4-glucano)-transferase [Saccharomyces cerevisiae] gi|171569|gb|AAA34632.1|[171569] 117: AAA23872 branching enzyme (EC 2.4.1.18) [Escherichia coli] gi|146142|gb|AAA23872.1|[146142] 118: AAA21151 beta-1,3 glucan transferase [Candida albicans] gi|532776|gb|AAA21151.1|[532776] 

We claim:
 1. An isolated DNA molecule encoding a fusion protein consisting of four different functional domains selected from the group consisting of GLASS, LINKR, GLYTR, and CTEND which are operably linked to one another.
 2. An isolated DNA molecule in claim 1, in which the GLASS domain comprises a GBSS GLASS.
 3. The isolated DNA molecule in claim 2 wherein the GBSS GLASS comprises a GLASS of SEQ ID NO: 1
 4. An isolated DNA molecule in claim 1, in which the GLASS domain comprises a SSI GLASS.
 5. The isolated DNA molecule of claim 4 wherein the SSI GLASS comprises a GLASS of SEQ ID NO: 2
 6. An isolated DNA molecule in claim 1, in which the GLASS domain comprises a SSII GLASS.
 7. The isolated DNA molecule of claim 6 wherein the SSII GLASS comprises a GLASS of SEQ ID NOs. 3 and 4
 8. An isolated DNA molecule in claim 1, in which the GLASS domain comprises a SSIII GLASS.
 9. The isolated DNA molecule of claim 8 wherein the SSIII GLASS comprises a GLASS of SEQ ID NO:5
 10. The isolated DNA molecule of claim 2, wherein said GBSS GLASS is a GLASS of a glucan producing organism.
 11. The isolated DNA molecule of claim 4, wherein said SSI-GLASS is a GLASS domain of a glucan producing organism.
 12. The isolated DNA molecule of claim 6, wherein said SSII-GLASS is a GLASS of a glucan producing organism.
 13. The isolated DNA molecule of claim 8, wherein said SSIII-GLASS is a GLASS of a glucan producing organism.
 14. The isolated DNA molecule of claim 2 wherein said GBSS-GLASS domain is at least 80% identical to a GLASS peptide of a glucan producing organism.
 15. The isolated DNA molecule of claim 4 wherein said SSI-GLASS domain is at least 80% identical to a GLASS peptide of a glucan producing organism.
 16. The isolated DNA molecule of claim 6 wherein said SSII-GLASS domain is at least 80% identical to a GLASS peptide of a glucan producing organism.
 17. The isolated DNA molecule of claim 8 wherein said SSIII-GLASS domain is at least 80% identical to a GLASS peptide of a glucan producing organism.
 18. An isolated DNA molecule of any of the claims in 2, 4, 6 or 8, in which the LINKR domain is a GBSS-LINKR, SSI-LINKR, SSII-LINKR or SSIII-LINKR.
 19. The isolated DNA molecule of claim 18 wherein said LINKR comprises a LINKR sequence selected from SEQ ID NOs:121-171; 336-386;527-577; 733-783; and 983-1033.
 20. An isolated DNA molecule of any of claims 2, 4, 6 or 8, in which the GLYTR domain is a GBSS-GLYTR, SSI-GLYTR, SSII-GLYTR or SSIII-GLYTR.
 21. An isolated DNA molecule of claim 18, in which the GLYTR is a GBSS-GLYTR, SSI-GLYTR, SSII-GLYTR or SSfi-GLYTR.
 22. The isolated DNA molecule of claim 20 wherein said GLYTR comprises a GLYTR sequence selected from SEQ ID NOs:1136, 1137, 1138, 1139, and
 1140. 23. The isolated DNA molecule of claim 21 wherein said GLYTR comprises a GLYTR sequence selected from SEQ ID NOs: 172-222; 387-437; 578-628; 784-834; and 1034-1084.
 24. An isolated DNA molecule of claims 2, 4, 6 or 8, in which the CTEND domain is a GBSS-CTEND, SSI-CTEND, SSII-CTEND or SSIII-CTEND.
 25. An isolated DNA molecule of claim 18, in which the CTEND domain is a GBSS-CTEND, SSI-CTEND, SSII-CTEND or SSIII-CTEND.
 26. An isolated DNA molecule of claim 20, in which the CTEND domain is a GBSS-CTEND, SSI-CTEND, SSII-CTEND or SSIII-CTEND.
 27. The isolated DNA molecule of claim 24 wherein said CTEND sequence comprises a CTEND sequence selected from SEQ ID NOs: 1146, 1147, 1148, 1148, 1149 and 1150
 28. The isolated DNA molecule of claim 25 wherein said CTEND sequence comprises a CTEND sequence selected from SEQ ID NOs:223-266; 438-461; 629-676; 835-882; and 1085-1135.
 29. The isolated DNA molecule of claim 26 wherein said CTEND sequence comprises a CTEND sequence selected from SEQ ID NOs: 223-266; 438-461; 629-676; 835-882; and 1085-1135.
 30. An isolated DNA molecule encoding a fusion peptide comprising a GBSS GLASS domain operably linked to a LINKR and a catalytic domain from a functional protein that synthesizes an α-1,4 glucan or an α-1,3 glucan, or an α-1,6 glucan, said fusion peptide being capable of modifying the glucan structure of a starch producing organism when starch is produced by said organism or part thereof in the presence of said fusion peptide.
 31. The DNA molecule of claim 30 wherein said fusion peptide comprises a GLASS and/or a LINKR sequence of SEQ ID NOs:75-120; 284-335, 475-526; 682-732; 933-982 and/or 121-171, 336-386, 527-577, 733-783, and 983-1033.
 32. An isolated DNA molecule encoding a polypeptide with glucan association properties of a maize GBSS enzyme capable of modification of starch metabolism in a plant or plant cell, said DNA comprising a molecule selected from the group consisting of: (a) a DNA molecule encoding a protein domain having the amino acid SEQ ID No.1 (b) a DNA molecule comprising a corresponding nucleotide sequence from SEQ ID No.1141 (c) a DNA molecule comprising a nucleotide sequence differing from the sequence of the DNA molecules of (a) or (b) due to the degeneracy of the genetic code, (d) a DNA molecule comprising a DNA sequence which hybridizes to any one of the DNA molecules of (a), (b) or (c) or fragment thereof, and which is equal to or more than 80% homologous or identical to the DNA molecule of (a), (b), or (c), or fragment thereof, wherein said DNA sequence encodes a polypeptide with Glucan Association Domain (Domain A) of a GBSS enzyme.
 33. An isolated DNA molecule encoding a polypeptide with a glycosyl transferase function of a soluble or granule bound maize SS enzymes capable of modifying starch metabolism in a plant or plant cell, said DNA molecule being selected from the group consisting of: (a) a DNA molecule encoding a protein domain comprising an amino acid of SEQ ID NOs:1, 2, 3, 4, and
 149. (b) a DNA molecule comprising the corresponding nucleotide sequence of SEQ ID NOs: 1141, 11142, 1143, 1144, and 1145, (c) a DNA molecule comprising a nucleotide sequence differing from the sequence of the DNA molecules of (a) or (b) due to the degeneracy of the genetic code, (d) a DNA molecule comprising a DNA sequence which hybridizes to any one of the DNA molecules of (a), (b) or (c), or fragment thereof, and which is equal to or more than 80% homologous or identical to the DNA molecule of (a), (b), or (c), or fragment thereof, wherein said DNA sequence encodes a polypeptide with a glycosyl transferase domain of a SS enzyme.
 34. A recombinant DNA molecule comprising a DNA molecule of any of the above claims comprising a maize GBSS nucleotide coding region encoding for an amino acid sequence of SEQ. ID NOs. 101-146 fused with a corresponding coding region of a maize SS enzyme that encode for an amino acid sequence of SEQ. ID NOs: 35-74; 121-171; 172-222; 223-266; 268-283; 284-335; 336-386; 387-437; 438-461; 463-474; 475-526; 527-577; 578-628; 629-676; 678-681; 682-732; 733-834; 835-882; 884-932; 933-982; 1034-1084; and 1085-1135.
 35. A recombinant DNA molecule comprising a DNA molecule of any of the above claims comprising a GLYTR, LINKR or CTEND domain DNA sequence selected from any one of SEQ ID NOs: 172-222; 387-437; 578-628; 784-834; 1034-1084, 121-171; 336-386; 527-577; 733-783; 983-1033 or 223-266; 438-461; 629-676; 835-882; 1085-1135 operably linked in any order with a corresponding DNA sequence that encodes for a glucan association domain from any one of SEQ ID NOs: 75-120; 284-335; 475-526; 682-732; 933-982.
 36. A recombinant DNA molecule comprising a DNA molecule of any of the above claims comprising a DNA sequence differing from the sequence of any of the DNA molecules of SEQ ID NOs: 34-1150 due to the degeneracy of the genetic code, and/or protein or polypeptide originating from a different source, such as a plant species other than plant species such as maize, bacteria (e.g. E. Coli), Yeast, algae (Chlamydomonas), or fungus.
 37. A recombinant DNA molecule comprising a DNA molecule of any of the above claims comprising a wherein the DNA sequence is selected from the group consisting of a coding region of a glucan association domain of SEQ ID NOs:75-120; 284-335; 475-526; 682-732; and 933-982 fused with a coding region of any glucan transferases listed in table XXXVII.
 38. Method of expressing a starch synthase fusion proteins or polypeptides in a plant, in which the starch synthase protein or polypeptide domains are expressed as a fusion with a glucan association domain of granule bound starch synthase. 39 A method according to any one of the preceding claims, in which the protein or polypeptide is heterologous with respect to the plant in which the fusion is expressed.
 40. Method according to any one of the preceding claims, comprising the steps of: providing a genetic construct comprising at least one nucleotide sequence encoding the desired protein domain or polypeptide domain combined with at least one nucleotide sequence encoding a glucan association domain of GBSS, so that the construct encodes a fusion of the desired protein/polypeptide and at least one glucan association domain; transforming a plant with said genetic construct; expressing said genetic construct in the plant.
 41. Method according to any one of the preceding claims in which the protein or polypeptide or recombinant protein or recombinant polypeptide is an enzyme.
 42. Method according to claim 41, in which the enzyme is an enzyme that can interact and associate with starch or starch granules, or facilitate or be entrapped in starch or starch granules, and is capable of at least one of modifying, increasing, decreasing, altering or influencing starch structure or starch synthesis.
 43. A vector comprising a DNA molecule according to any of the preceding claims.
 44. A vector according to claim 43, wherein the DNA molecule is linked in sense orientation to DNA elements ensuring transcription of a translatable RNA in a prokaryotic or an eukaryotic cell.
 45. A host cell comprising a vector according to claim
 43. 46. A plant cell comprising a DNA molecule according to any one of the preceding claims linked to a heterologous promoter.
 47. A plant comprising a plant cell according to claim
 46. 48. The plant of claim 47, which is a cereal, such as maize, rice, wheat, barley, oats, or a root crop, such as potato, sweet potato, cassaya, yam, taro, or other starch producing plant, such as peas or banana.
 49. A plant according to claim 47 wherein said plant contains or produces starch or starch granules in at least one of its parts, including its seeds, leaves, roots (tubers), tubers, stems, stalks, fruits, grains or flowers.
 50. A plant according to claim 49 wherein said elements include a homologous or heterologous promoter specific for expression of said DNA molecule in said at least one of its parts.
 51. A seed from the plant of claim 49, capable of expressing said recombinant molecule.
 52. A modified starch derived from cells of a plant of any of the preceding claims.
 53. Food or feed comprising a modified starch of claim
 52. 